Program for managing hand osteoarthritis
A Protocol for a Randomised Controlled Pilot and Feasibility Study
This study is testing a new program to help people with hand osteoarthritis improve their daily activities and see if it works well in real life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 32 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Parker Research Institute Academic / other |
| Locations | 1 site (Copenhagen, Capital Region) |
| Trial ID | NCT06794632 on ClinicalTrials.gov |
What this trial studies
This pilot study investigates the feasibility of the HANDY program, designed for individuals with hand osteoarthritis, focusing on improving their ability to perform daily activities. The program incorporates occupational therapy interventions and is being tested in collaboration with two municipalities in Denmark. The study aims to evaluate recruitment and retention procedures, acceptance of the program in practice, and the appropriateness of assessment tools used during group interventions. The findings will inform the planning of a full-scale randomized controlled trial.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 diagnosed with hand osteoarthritis who experience difficulties in daily activities.
Not a fit: Patients with severe vision or hearing loss, cognitive deficits, or acute illnesses affecting their ability to engage in the program may not benefit.
Why it matters
Potential benefit: If successful, this program could significantly enhance the daily functioning and quality of life for patients with hand osteoarthritis.
How similar studies have performed: While there is limited rigorous research on occupational therapy for hand osteoarthritis, similar interventions have shown promise in improving daily living activities in other chronic conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * People diagnosed by general practitioner with hand osteoarthritis * Aged \> 18 years * Experiencing decreased ADL ability Exclusion Criteria: * Severe vision loss * Severe hearing loss * Cognitive deficits affecting the ability to engage in peer-learning activities * Unable to participate in two or more group sessions due to other scheduled activities (e.g. holidays/travels). * Acute illness is the primary reason for decreased ADL ability (Will be referred to other services in the municipality).
Where this trial is running
Copenhagen, Capital Region
- The Parker Institute — Copenhagen, Capital Region, Denmark (Recruiting)
Study contacts
- Study coordinator: Ulla Andersen, Master of occupational therapy
- Email: ulla.andersen.03@regionh.dk
- Phone: 004520286578
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.