Feasibility and acceptability of instructions of daily care in overweight and obese knee osteoarthritis participants

• Main Authors: Rafiq, Muhammad T., Hamid, Mohamad Shariff A., Hafiz, Eliza, Chaudhary, Farid A., Khan, Muhammad I.
• Format: Article
• Published: Bentham Science Pub. 2021
• Subjects: RC1200 Sports Medicine; RL Dermatology
• Online Access: http://eprints.um.edu.my/35634/; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85113169734&doi=10.2174%2f1573397117666210727095552&partnerID=40&md5=7c4eda52bc266f9771d579571076646f
• Institution: Universiti Malaya

Knee Osteoarthritis (OA) is a weight-bearing joint disease and is more common in overweight and obese persons. The objective of the study was to assess the feasibility and acceptability of Instructions of Daily Care (IDC) on pain, mobility, and Body Mass Index (BMI) among knee OA participants who are overweight or obese. Materials and Methods: The study was an open-label randomized controlled trial of six weeks. Forty overweight and obese participants with knee OA were randomly divided into two groups by a computer-generated number. The participants in the Instruction Group (IG) were provided with leaflets explaining IDC for the duration of six weeks. Both groups were instructed to take low doses of the non-steroid anti-inflammatory drug (NSAIDs) on alternate days. The outcome measures were pain, mobility and BMI. The feasibility and acceptability of knee pain and mobility were assessed using a questionnaire designed by experts in rehabilitation. Results: Participants in the IG reported more statistically significant pain relief as assessed by the Western Ontario and McMaster Universities Osteoarthritis Index score (p=0.001) and improvement in mobility (p=0.000) assessed by the Timed Up and Go test score after six weeks compared to the Control Group (CG). Both groups did not demonstrate any significant change in BMI (p-value > 0.05). The results of descriptive statistics showed a significantly higher satisfaction score for participants who received a combination of IDC and NSAIDs, indicating an acceptable intervention. Conclusion: The IDC is effective and acceptable in terms of improving pain and mobility and should be recommended as the usual care of treatment. Clinical Trial Registration Number: Chinese Clinical Trial Registry with registration number ChiCTR2000034163. © 2021 Bentham Science Publishers.