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About
The goal of the trial is to test the usability, feasibility and acceptability of an unsupervised, appbased yoga program for participants undergoing thoracic RT and their caregivers.
Full description
Primary Objective:
The Investigators propose to test the usability, feasibility and acceptability of an unsupervised, app-basedyoga program for patients undergoing thoracic RT and their caregivers. The Investigators specific aims will be carried out in two parts:
Part 1:
• The Investigators will perform the initial usability testing of the working prototypes of both iOS and Android versions to determine whether users can complete the required tasks successfully and independently and to identify problems with navigation and functioning.
The Investigators primary objective is to:
Aim 1: Finalize the working prototype of the yoga app using the feedback of 10 participants-caregiver dyads (mixed-methods study).
Part 2:
• The Investigators will measure feasibility (e.g., consent and retention rates, adherence), usability of the app, and acceptability of the app-based program in 20 newly recruited participants-caregiver dyads. As an exploratory outcome, the investigators include pre- and post-intervention assessments of objective physical function and self-reported QOL. The Investigators will also complete semi-structured interviews to collect qualitative data on participants' evaluation of the mobile app and their experience in participating in this research.
Specific aims are:
Aim 1: Examine the feasibility, usability, and acceptability of an app-based yoga program in 20 patient-caregiver dyads (single-arm trial).
Aim 2: Understand the trial participants' experiences with the mobile app delivery including suggestions for improvement using qualitative methods.
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Inclusion criteria
Both patient and caregiver must meet all the following criteria:
Exclusion criteria
Participants who participated in part 1 are ineligible to participate in part 2 of this protocol.
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Interventional model
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60 participants in 1 patient group
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Central trial contact
Kathrin Milbury, MA,PHD
Data sourced from clinicaltrials.gov
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