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I am currently running SPSS 18. I am trying to determine
the best way to use SPSS to analyze our data on remote telemonitoring of blood
pressure. For any individual, I can see a trend though there is a great deal
of variability in the data on blood pressure. I may have up to 900
observations over a period of months on an individual and I have 150
individuals in the pilot study. The number of observations per individual is
too great for the repeated measures ANOVA, but I believe I have to account for
the lack of independence in the analysis. Any ideas would be helpful. Thanks! Healthy Regards,
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Allen,
Please, Talk more about the purpose of the study? The variability is an aspect to be considered by itself? bye bye Luciano Basso ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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The purpose of the study is to assess the impact that remote telemonitoring has on an individual's ability to help manage blood pressure. Blood pressure readings are taken multiple times a day and remotely uploaded to our system so that a health coach can reach out to the individual if the blood pressure gets dangerously high or out of control. What we are seeing is that an individual's blood pressure has tremendous fluctuations throughout the day, and the number of observations per individual is complicating the analysis.
-----Original Message----- From: luciano basso [mailto:[hidden email]] Sent: Friday, January 22, 2010 1:40 PM To: Allen Frommelt Cc: [hidden email] Subject: Re: Question on analysis--many observations per subject Allen, Please, Talk more about the purpose of the study? The variability is an aspect to be considered by itself? bye bye Luciano Basso This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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Allen Frommelt wrote:
> The purpose of the study is to assess the impact that remote > telemonitoring has on an individual's ability to help manage blood > pressure. Blood pressure readings are taken multiple times a day and > remotely uploaded to our system so that a health coach can reach out > to the individual if the blood pressure gets dangerously high or out > of control. What we are seeing is that an individual's blood > pressure has tremendous fluctuations throughout the day, and the > number of observations per individual is complicating the analysis. There are still a lot of unanswered questions. Is there a concurrent control group? Do you have measurements prior to the intervention? Are there any covariates that you need to adjust for? Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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There are still a lot of unanswered questions. Is there a concurrent
control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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Allan,
Is context for the questions you asked an ongoing, real-time blood pressure monitoring process where a person's incoming data is 'processed' in some manner to identify when a coach needs to contact the person for some sort of intervention work? By 'real-time' I mean that the person's blood pressure data are uploaded, either manually or by an automated data link, either immediately or at short, but regular intervals. OR, is this a completed data collection project in which the data have already been collected and are now to be analyzed. If the former, does each person have a predefined blood pressure threshhold (e.g., 140/100) that trigger a coaching contact? Or, is the threshold a pattern of blood pressure readings that occur over a day, several days or weeks? Gene Maguin -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Friday, January 22, 2010 3:22 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject There are still a lot of unanswered questions. Is there a concurrent control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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The pilot is ongoing, but I'm trying to come up with ideas for the analysis based on how things are starting to be collected and looking at the large number of readings. The blood pressure data is uploaded through an automated data link. There is a predefined blood pressure threshold that triggers an alert.
Allen -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Gene Maguin Sent: Friday, January 22, 2010 3:42 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject Allan, Is context for the questions you asked an ongoing, real-time blood pressure monitoring process where a person's incoming data is 'processed' in some manner to identify when a coach needs to contact the person for some sort of intervention work? By 'real-time' I mean that the person's blood pressure data are uploaded, either manually or by an automated data link, either immediately or at short, but regular intervals. OR, is this a completed data collection project in which the data have already been collected and are now to be analyzed. If the former, does each person have a predefined blood pressure threshhold (e.g., 140/100) that trigger a coaching contact? Or, is the threshold a pattern of blood pressure readings that occur over a day, several days or weeks? Gene Maguin -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Friday, January 22, 2010 3:22 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject There are still a lot of unanswered questions. Is there a concurrent control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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I realize I asked questions that others had asked and you already had
answered. Apologies. I'm thinking that a person's data could be thought of as consisting of multiple series of observations in which blood pressure is within limits and separated by one or more series of observations in which blood pressure exceeded limits and triggered an intervention. Thought about in this way, there are several variables that could be constructed but a main one might be segments consisting of a certain number of observations bracketing the threshold event. It would seem that a three level model could be set up in which level 1 models the blood pressure observations. The level 1 model could be as simple the difference of the pre and post means, or a function of some covariates and an intervention marker (0,1). I don't know anything about blood pressure so I have no idea what would be relevant. Level 2 would be occasion and which refers to the instances of intervention. Level 3 would be persons. I'd thought about using a strategy like this for another project but the project never started. I can point to no examples of an analysis like this and there may be obvious problems that I don't see. I'm guessing that you'd like to see that the intervals between intervention instances increases over time for each person and that the impact of an intervention either remains the same over time or increases in magnitude (i.e., a greater and/or quicker blood pressure decrease). -----Original Message----- From: Allen Frommelt [mailto:[hidden email]] Sent: Friday, January 22, 2010 3:49 PM To: Gene Maguin; [hidden email] Subject: RE: Question on analysis--many observations per subject The pilot is ongoing, but I'm trying to come up with ideas for the analysis based on how things are starting to be collected and looking at the large number of readings. The blood pressure data is uploaded through an automated data link. There is a predefined blood pressure threshold that triggers an alert. Allen -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Gene Maguin Sent: Friday, January 22, 2010 3:42 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject Allan, Is context for the questions you asked an ongoing, real-time blood pressure monitoring process where a person's incoming data is 'processed' in some manner to identify when a coach needs to contact the person for some sort of intervention work? By 'real-time' I mean that the person's blood pressure data are uploaded, either manually or by an automated data link, either immediately or at short, but regular intervals. OR, is this a completed data collection project in which the data have already been collected and are now to be analyzed. If the former, does each person have a predefined blood pressure threshhold (e.g., 140/100) that trigger a coaching contact? Or, is the threshold a pattern of blood pressure readings that occur over a day, several days or weeks? Gene Maguin -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Friday, January 22, 2010 3:22 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject There are still a lot of unanswered questions. Is there a concurrent control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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In reply to this post by Allen Frommelt
If the goal of the analysis is patient monitoring it seems like you should be looking at the approaches that businesses use for monitoring manufacturing processes. They take repeated samples, several times per day/hour and adjust the machinery once some threashold is exceeded. (That's all I remember, you'll need to talk to someone else for more detail.)
Noisy data might benefit from some sort of data smoothing. For example a moving average might provide a stable representation of longer term trends in an individual's blood pressure. Or am I misunderstanding the goal? Michael **************************************************** Michael Granaas [hidden email] Assoc. Prof. Phone: 605 677 5295 Dept. of Psychology FAX: 605 677 3195 University of South Dakota 414 E. Clark St. Vermillion, SD 57069 ***************************************************** ________________________________________ From: SPSSX(r) Discussion [[hidden email]] On Behalf Of Allen Frommelt [[hidden email]] Sent: Friday, January 22, 2010 2:49 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject The pilot is ongoing, but I'm trying to come up with ideas for the analysis based on how things are starting to be collected and looking at the large number of readings. The blood pressure data is uploaded through an automated data link. There is a predefined blood pressure threshold that triggers an alert. Allen -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Gene Maguin Sent: Friday, January 22, 2010 3:42 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject Allan, Is context for the questions you asked an ongoing, real-time blood pressure monitoring process where a person's incoming data is 'processed' in some manner to identify when a coach needs to contact the person for some sort of intervention work? By 'real-time' I mean that the person's blood pressure data are uploaded, either manually or by an automated data link, either immediately or at short, but regular intervals. OR, is this a completed data collection project in which the data have already been collected and are now to be analyzed. If the former, does each person have a predefined blood pressure threshhold (e.g., 140/100) that trigger a coaching contact? Or, is the threshold a pattern of blood pressure readings that occur over a day, several days or weeks? Gene Maguin -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Friday, January 22, 2010 3:22 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject There are still a lot of unanswered questions. Is there a concurrent control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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In reply to this post by Allen Frommelt
Hi Allen,
I occasionally work with blood glucose data from continuous glucose monitoring systems, which provide readings every 5 minutes. Usually we collect data for 72 hours at a time. Our approach is to define a number of summary measures depending on the research questions. For example, area under the curve, time spent above 12 mmol/L, peak value, variability indices, mean value in the half hour before each meal, mean value in the 4 hours after each meal, etc. For your study I would recommend considering something similar - identify what characteristics (eg, mean levels, variability, excursions, number of times the threshold is reached) of blood pressure you are interested in and what summaries can be used to measure them. Simplifying the data to a small number of summary measures will be a big help in tackling this much data. Cheers, Kylie. -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Saturday, 23 January 2010 7:19 AM To: [hidden email] Subject: Re: Question on analysis--many observations per subject The pilot is ongoing, but I'm trying to come up with ideas for the analysis based on how things are starting to be collected and looking at the large number of readings. The blood pressure data is uploaded through an automated data link. There is a predefined blood pressure threshold that triggers an alert. Allen -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Gene Maguin Sent: Friday, January 22, 2010 3:42 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject Allan, Is context for the questions you asked an ongoing, real-time blood pressure monitoring process where a person's incoming data is 'processed' in some manner to identify when a coach needs to contact the person for some sort of intervention work? By 'real-time' I mean that the person's blood pressure data are uploaded, either manually or by an automated data link, either immediately or at short, but regular intervals. OR, is this a completed data collection project in which the data have already been collected and are now to be analyzed. If the former, does each person have a predefined blood pressure threshhold (e.g., 140/100) that trigger a coaching contact? Or, is the threshold a pattern of blood pressure readings that occur over a day, several days or weeks? Gene Maguin -----Original Message----- From: SPSSX(r) Discussion [mailto:[hidden email]] On Behalf Of Allen Frommelt Sent: Friday, January 22, 2010 3:22 PM To: [hidden email] Subject: Re: Question on analysis--many observations per subject There are still a lot of unanswered questions. Is there a concurrent control group? [Allen Frommelt: Yes] Do you have measurements prior to the intervention?[Allen Frommelt: Yes] Are there any covariates that you need to adjust for?[Allen Frommelt: I don't know that they have all been identified yet] Still, as a general piece of advice, there are two things you could do. 1. Simplify the model by averaging. Compute a preintervention mean and a postintervention mean for each subject and then run a paired t-test. Or compute a postintervention mean for every subject in your treatment group and a postintervention mean for every subject in your control group and then use these means as the raw data for a two sample t-test. 2. Learn how to run a mixed model. Averaging sometimes throws information away, but it also produces a data set where the statistic of choice is obvious. Mixed models are messy, but they allow for examination of relationships and patterns that might otherwise get missed with a simpler model. -- Steve Simon, Standard Disclaimer "What do all these numbers mean? Sensitivity, specificity, and likelihood ratios" Wednesday, February 17, 11am-noon, CST Free to all! www.pmean.com/webinars This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD This email and all attachments are confidential and intended solely for the use of the individual or entity to which they are addressed. If you have received this email in error please notify the sender by replying to this message. If you are not the intended recipient, please delete this message and all attachments immediately. Do not copy, disclose, use or act upon the information contained. Please note that any views or opinions presented in this email are solely those of the author and do not necessarily represent those of the company. Finally, the recipient should check this email and any attachments for the presence of viruses. While every attempt is made to verify that the contents are safe, the company accepts no liability for any damage caused by any virus transmitted by this email. ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD ===================== To manage your subscription to SPSSX-L, send a message to [hidden email] (not to SPSSX-L), with no body text except the command. To leave the list, send the command SIGNOFF SPSSX-L For a list of commands to manage subscriptions, send the command INFO REFCARD |
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