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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05559255 -
Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI
|
N/A | |
Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
Completed |
NCT05057988 -
Virtual Empowered Relief for Chronic Pain
|
N/A | |
Completed |
NCT04466111 -
Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
|
||
Recruiting |
NCT06206252 -
Can Medical Cannabis Affect Opioid Use?
|
||
Completed |
NCT05868122 -
A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy
|
Phase 3 | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Enrolling by invitation |
NCT06087432 -
Is PNF Application Effective on Temporomandibular Dysfunction
|
N/A | |
Completed |
NCT05508594 -
Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001
|
Phase 2/Phase 3 | |
Recruiting |
NCT03646955 -
Partial Breast Versus no Irradiation for Women With Early Breast Cancer
|
N/A | |
Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
Completed |
NCT03678168 -
A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries
|
N/A | |
Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
Completed |
NCT03931772 -
Online Automated Self-Hypnosis Program
|
N/A | |
Completed |
NCT02913027 -
Can We Improve the Comfort of Pelvic Exams?
|
N/A | |
Terminated |
NCT02181387 -
Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor?
|
Phase 4 | |
Recruiting |
NCT06032559 -
Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment
|
Phase 3 | |
Active, not recruiting |
NCT03613155 -
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
|