This feasibility study will evaluate yoga as a treatment for chronic musculoskeletal pain. The experimental treatment is yoga delivered via a tablet computer to participants at home ("teleyoga"). First, the investigators will develop a suitable protocol for teleyoga. Second, the investigators will demonstrate the feasibility of conducting a randomized controlled trial involving randomization to teleyoga or in-person yoga groups.
The first phase of the study is not randomized. In this phase, the first group of participants (n=10) will all participate in a tele-yoga class using an iPad loaned to them by the study. They will attend this treatment session from the comfort of their home or a location of their choice. Yoga treatment will last 12 weeks. At the end of treatment, veterans will provide feedback by completing a satisfaction questionnaire to rate various aspects of the teleyoga (e.g. technical challenges, ability to perform yoga through the video-conferencing platform, problems that occurred, and recommendations to improve the class, etc). The teleyoga protocol will be modified on the basis of this feedback and will be tested on a second group of participants (n=10). The second phase of the study will involve randomization of a further group of participants (n=30) to either the teleyoga developed in phase one, or in-person yoga.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
34
the yoga protocol will be delivered via a tablet computer to groups of participants
the yoga protocol will be delivered by a yoga instructor in the room to group of participants
VA Palo Alto Health Care System
Palo Alto, California, United States
Multi-Dimensional Treatment Satisfaction Measure
A participant satisfaction measure \[score range: 0 to 4\]. The higher the value, the greater the treatment satisfaction
Time frame: after 12 weeks of treatment
Adherence to the Treatment Protocol
% of randomized patients who attend ≥65% of treatment sessions
Time frame: during 12 weeks of treatment
Attrition
number of randomized patients who drop out of treatment
Time frame: during 12 weeks of treatment
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