Embedding Ehealth Trials in Clinical Practice
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Abstract
Background: Despite claims that internet treatments for psychological conditions might be used alongside i.e. contemporaneous with clinical treatment, as opposed to preventation, early intervention, non-clinical, or post treatment populations, the logistics, ethics, feasibility and acceptabilty of undertaking such a trial in a help seeking and clinician treated population has little evidential guidance.
Objective - To describe the logistic and ethical issues raised in conducting ehealth trials in "patient" populations from the researcher's view point and the feasibility, acceptability and adherence issues from a qualitative study of trial participants
Methods: SOMNA is an RCT comparing internet based CBT for insomnia (Shuti) with an active internet control conditon as an adjunctive treatment for depression in older men. The participants all receive psychiatrist coordinated guideline based treament for their depression for three months and are randomly allocated to one arm for a nine week intervention period with pre post assessments of psychological and phsyical health and sleep paramaters including actigraphy.
The logistical and ethical issues in embedding such a trial, rather than the internet-based logistics in most such intervetniosn, have been recorded by the research team
So far 46 participants have been recruited and randomised. A qualitative study by a blinded researcher of a subset of these is underway to evaluate participant engagement in this setting
Results: Research in progress.
Conclusions: Research in progress but these will inform future ehealth-clinical interfaces
Objective - To describe the logistic and ethical issues raised in conducting ehealth trials in "patient" populations from the researcher's view point and the feasibility, acceptability and adherence issues from a qualitative study of trial participants
Methods: SOMNA is an RCT comparing internet based CBT for insomnia (Shuti) with an active internet control conditon as an adjunctive treatment for depression in older men. The participants all receive psychiatrist coordinated guideline based treament for their depression for three months and are randomly allocated to one arm for a nine week intervention period with pre post assessments of psychological and phsyical health and sleep paramaters including actigraphy.
The logistical and ethical issues in embedding such a trial, rather than the internet-based logistics in most such intervetniosn, have been recorded by the research team
So far 46 participants have been recruited and randomised. A qualitative study by a blinded researcher of a subset of these is underway to evaluate participant engagement in this setting
Results: Research in progress.
Conclusions: Research in progress but these will inform future ehealth-clinical interfaces
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