Status:

COMPLETED

The Effects of a Knitting Program on Osteoarthritis Symptoms in Elderly Women

Lead Sponsor:

Université de Sherbrooke

Collaborating Sponsors:

University of Ottawa

Conditions:

Osteoarthritis

Eligibility:

FEMALE

50-85 years

Phase:

NA

Brief Summary

This pilot randomized controlled trial (RCT) studies the adherence and clinical effectiveness of a knitting program in older females suffering from hand osteoarthritis (HOA) to evaluate the acceptabil...

Detailed Description

Background: Exercise therapy is effective in reducing symptoms and disability associated with hand osteoarthritis (HOA) but has low adherence. An intervention consisting in a meaningful occupation, su...

Eligibility Criteria

Inclusion

  • Meet the clinical and radiographic criteria of definite HOA set out by the American College of Rheumatology (ACR) and have experienced pain symptoms for at least 3 months;
  • Be a woman aged between 50 and 85 years; 3) have moderate to severe morning stiffness (defined as a score ≥ 4 on a 10 cm visual analogue scale at the time of study entry;
  • Display X-ray evidence of joint space narrowing of the hands;
  • Have no previous experience with knitting or have not knitted in the last 6 months;
  • Be available for sessions at the senior's club twice weekly;
  • Be able to understand written and verbal English instructions.

Exclusion

  • Suffered from other orthopedic or rheumatologic diseases (e.g., inflammatory arthritis), or showed evidence of chondrocalcinosis;
  • Had a history of finger joint surgery;
  • Suffered from an acute disease, such as uncontrolled diabetes mellitus, untreated hypertension, neurological deficits (motor or sensory), cognitive deficit or mental health conditions;
  • Were taking OA medication that was expected to change during the study period;
  • Were receiving current rehabilitation treatments or any other pain-related treatment besides medication for OA;
  • Had received a corticosteroid injection in a finger joint within the last 6 months;
  • Planned to move outside the region within 6 months.

Key Trial Info

Start Date :

August 1 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 20 2017

Estimated Enrollment :

37 Patients enrolled

Trial Details

Trial ID

NCT05975229

Start Date

August 1 2017

End Date

December 20 2017

Last Update

August 3 2023

Active Locations (1)

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1

University of Ottawa

Ottawa, Quebec, Canada