Actively Recruiting

Phase Not Applicable
All Genders
ID07055113

Adapting Rehabilitation Delivery for Maximum Impact at Home-2 (ReDI-2) Comparing Virtual Individual and Group Physical Therapy for Rural Hip or Knee Osteoarthritis

Led by University of Alberta · Updated on 2025-08-26

270

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

C

Canadian Institutes of Health Research (CIHR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating two virtual physical therapy programs for people living in rural areas with hip or knee osteoarthritis (OA). The study compares usual community-based OA care with two 12-week home-based virtual rehabilitation programs: Individual Physical Therapy (IPT) and Group-based Physical Therapy (GPT). The goal is to improve how patients manage their OA by increasing their activation and involvement in self-care through education, exercise, and personalized goals. Participants will first continue with usual OA care for 12 weeks, followed by randomization to either IPT or GPT programs. Both programs are delivered weekly via Zoom over 12 weeks, with a break after 6 weeks to encourage independent management. IPT involves one-on-one virtual sessions with a physiotherapist, while GPT includes group classes of 4-5 participants led by two physiotherapists, with private breakout sessions for personalized goal-setting. The interventions include education on OA management, pain control, healthy living, mental well-being, and tailored neuromuscular exercises with resistance bands and Fitbit step goals. Participants will be assessed at multiple points: before usual care, before intervention, immediately after, and at 6 and 12 months post-intervention. Assessments include patient activation, pain, quality of life, physical function, and activity levels measured by Fitbit. The study uses secure Zoom sessions with technology support provided. Researchers will track progress and adherence through questionnaires, physical performance tests, and Fitbit data to evaluate the impact of the programs on OA self-management and overall health.

CONDITIONS

Brief Title

Adapting Rehabilitation Delivery for Maximum Impact at Home-2 (ReDI-2)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with confirmed hip or knee osteoarthritis not requiring total joint replacement (not on surgical waitlist)
  • Not currently attending physiotherapy
  • Reside outside of Edmonton or nearby communities (rural area)
  • English-speaking
  • Access to a Zoom-compatible device such as smartphone, tablet, or laptop
Not Eligible

You will not qualify if you...

  • Patients who do not meet the inclusion criteria are not eligible

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Usual Care Observation

Duration - 12 weeks

Participants receive 12 weeks of community-based usual care for osteoarthritis, including educational materials and any treatments they independently seek. This period is observed to assess the impact of usual care before starting the virtual therapy programs.

Assessments before and after 12 weeks of usual care

Virtual Physical Therapy

Duration - 12 weeks

Participants are randomized to receive one of two 12-week virtual home-based rehabilitation programs: Individual Physical Therapy (IPT) with weekly one-on-one sessions or Group-based Physical Therapy (GPT) with weekly group sessions including personalized breakout room interactions. The program includes education, personalized goal setting, and progressive exercises with encouragement to exercise between sessions.

Weekly virtual sessions for 6 weeks, 2-week break, return at week 9, and an optional check-in at week 12

Follow-up Assessments

Duration - Up to 12 months post-intervention

Participants are assessed at immediate post-intervention, and at 6- and 12-months post-intervention to evaluate long-term outcomes including self-management, pain, function, and physical activity.

Assessments at immediate post-intervention, 6 months, and 12 months post-intervention

Trial Site Locations

Total: 1 location

1

Edmonton Bone and Joint Centre

Edmonton, Alberta, Canada

Actively Recruiting

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Research Team

L

Lauren Beaupre, PT, PhD

A

Ailar Ramadi, PT, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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