Pain Clinical Trial
Official title:
Protocol for a Pilot Randomized Controlled Trial of the Evaluation of Yoga and Aerobic Dance for Pain Management in Juvenile Idiopathic Arthritis
The primary objectives of the proposed pilot randomized controlled trial (RCT) will be to examine: (1) the feasibility of a full RCT to evaluate the effectiveness of two popular types of physical activity (PA), a yoga training program and an aerobic dance training program, in female adolescents (13 to 18 years old) with juvenile idiopathic arthritis (JIA) compared to a wait list control group; and (2) the acceptability of these interventions. A three-arm prospective randomized open-label study with a parallel group design will be used. A total of 25 in a ratio of 2:2:1 female adolescents with JIA who have pain will be randomized to one of the three groups: 1) online yoga training program (Group A) (n=10), 2) online aerobic dance training program (Group B) (n=10) and 3) waiting list control group (Group C) (n=5). Participants in groups A and B will complete three individual 1-hour sessions per week using online exercise videos, as well as one 1-hour virtual group session per week using a video-conferencing platform (GoToMeeting) for 12 weeks. These participants will also take part in weekly e-consultations with a research coordinator and discussions on Facebook with other participants. Participants from all groups will be given access to an electronic educational pamphlet on PA for arthritis developed by The Arthritis Society to review via an online platform. Feasibility, acceptability and usability of Facebook and GoToMeeting will be assessed at the end of the program. Pain intensity (Primary outcome), participation in general physical activity, morning stiffness, functional status, fatigue, self-efficacy and patient global assessment will be assessed using self-administered electronic surveys at baseline, weekly until the end of the 12 weeks program.
Objectives: The primary objectives of the proposed pilot randomized controlled trial (RCT)
will be to examine: (1) the feasibility of a full RCT to evaluate the effectiveness of two
popular types of physical activity (PA), a yoga training program and an aerobic dance
training program, in female adolescents (13 to 18 years old) with juvenile idiopathic
arthritis (JIA) compared to a wait list control group; and (2) the acceptability of these
interventions.
Methods: A three-arm prospective randomized open-label study with a parallel group design
will be used. A total of 25 female adolescents with JIA who have pain will be randomized in a
ratio of 2:2:1 to one of the three groups: 1) online yoga training program (Group A) (n=10),
2) online aerobic dance training program (Group B) (n=10) and 3) wait list control group
(Group C) (n=5). Participants in groups A and B will complete three individual 1-hour
sessions per week using online exercise videos, as well as one 1-hour virtual group session
per week using a video-conferencing platform (GoToMeeting) for 12 weeks. These participants
will also take part in weekly e-consultations with a research coordinator and discussions on
Facebook with other participants. Participants from all groups will be given access to an
electronic educational pamphlet on PA for arthritis developed by The Arthritis Society to
review via an online platform. Feasibility (recruitment rates, self-reported adherence to the
interventions, dropout rates, and percentage of missing data), acceptability and usability of
Facebook and GoToMeeting will be assessed at the end of the program. Pain intensity (Primary
outcome), participation in general physical activity, morning stiffness, functional status,
fatigue, self-efficacy and patient global assessment will be assessed using self-administered
electronic surveys at baseline, weekly until the end of the 12 weeks program.
Conclusion: To our knowledge this is the first study in paediatric patients to evaluate the
effectiveness of yoga and aerobic dance as pain management interventions for female
adolescents with JIA. The use of online tools such as Facebook and GoToMeeting to disseminate
these two PA interventions may facilitate access to alternative methods of pain management in
this population. The study design incorporates randomization and allocation concealment to
ensure internal validity. To avoid intergroup contamination, the Facebook group page security
settings will be set to "closed", thus only allowing invited participants to access it. Study
limitations include the lack of participant blinding due to the characteristics of this
physical intervention pilot randomized controlled trial and a potential bias of recruiting
more severe hospital-based participants. Reporting of the study follows the Standard Protocol
Items: Recommendations for interventional trials (SPIRIT) statement. This study can lead to a
full-scale RCT.
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