Effectiveness of an Internet-Delivered Exercise and Pain-Coping Skills Training Intervention for Persons With Chronic Knee Pain: A Randomized Trial.
Kim L Bennell, Rachel Nelligan, Fiona Dobson...
https://pubmed.ncbi.nlm.nih.gov/28241215/Actively Recruiting
Led by Cairo University · Updated on 2026-03-02
68
Participants Needed
1
Research Sites
21 weeks
Total Duration
Researchers are comparing three different physical therapy delivery methods to treat adults aged 20 to 40 years with chronic non-specific neck pain lasting three months or longer. The study aims to find out which approachtele-rehabilitation, face-to-face exercises, or a mixed modelis most effective at reducing neck pain and improving function. It also examines differences in neck movement, fear of movement, patient satisfaction, and adherence to exercise programs. Participants are randomly assigned to one of three groups real-time video-guided tele-rehabilitation sessions conducted at home with live physiotherapist supervision traditional in-person supervised sessions at a clinical facility or a hybrid model alternating weekly between in-person and tele-rehabilitation sessions. Each participant completes a structured exercise program that lasts 45-60 minutes per session, three times a week, for six weeks. The exercises progress through phases focusing on mobility, pain reduction, strengthening, and endurance. During the study, participants undergo assessments at the start, immediately after the 6-week intervention, and again at 3 months post-treatment. These assessments measure neck pain intensity, functional disability, cervical range of motion, fear of movement, patient satisfaction, and adherence to the exercise program. The study tracks progress continuously throughout the 6-week period, aiming to understand how different delivery methods affect recovery and long-term outcomes.
CONDITIONS
Telerehabilitation, Face-to-Face Exercises, and a Mixed Model in Chronic Non-Specific Neck Pain
A
Amr Ahmad Fallatah, Doctoral
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Cairo University
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote depending on site procedures)
Duration - 6 weeks
Participants receive one of three exercise interventions: real-time video-guided tele-rehabilitation sessions, in-person supervised exercise sessions, or a hybrid model combining both approaches. Sessions occur three times per week for 6 weeks with live physiotherapist supervision.
3 sessions per week (45-60 minutes each), delivered via video conferencing or in-person depending on assigned group
Duration - 3 months post-treatment
Participants are assessed for functional disability, neck pain intensity, range of motion, kinesiophobia, and patient satisfaction after completing the intervention, with additional monitoring at 3 months post-treatment.
1 visit within 1 week post-treatment and 1 visit at 3 months post-treatment
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Kim L Bennell, Rachel Nelligan, Fiona Dobson...
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https://pubmed.ncbi.nlm.nih.gov/37770963/Isabel Audette, Jean-Pierre Dumas, Julie N Côté...
https://pubmed.ncbi.nlm.nih.gov/20436238/Cairo University
Lead Sponsor