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Life-Style Medicine for Chronic Musculoskeletal Pain in Older People: A Pragmatic, Randomized Controlled Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to determine the clinical effectiveness of lifestyle medicine in reducing chronic musculoskeletal pain in older adults, as measured by pain intensity, pain interference, self-management efficacy, stress level, sleep quality, healthier diet, better quality of life, and cost-effectiveness, compared to a waitlist control group. Participants will be randomly assigned to either the intervention or the waitlist group. The intervention group will meet the health coach face-to-face for four sessions to negotiate and set personalized health goals. The waitlist control group will continue to receive usual care without any additional intervention for 24 weeks. Both groups will complete three assessments: at the start of the study, one month after the intervention, and three months after the intervention. The waitlist control group will be offered the same intervention after completing the study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Healthy Volunteers: f
View:

• chronic musculoskeletal pain, defined as pain that lasted for more than 3 months persistently or intermittently, including regional pain (joints, limbs, back, and/or neck)

• a degenerative joint condition, such as osteoarthritis, and/or musculoskeletal complaints that fall under the classification of the International Classification of Disease-11 as chronic primary musculoskeletal pain or chronic secondary musculoskeletal pain

• Pain intensity score ≥ 4 on a numerical rating scale of 10

• stable baseline physical activity

• ability to understand written and verbal Chinese

Locations
Other Locations
Hong Kong Special Administrative Region
4/F, Lek Yuen Health Center, Shatin, New Territories, Hong Kong
RECRUITING
Hong Kong
Contact Information
Primary
Cheryl Fung, Bachelor
cheryllcfung@cuhk.edu.hk
+852 2609 5050
Time Frame
Start Date: 2025-02-09
Estimated Completion Date: 2027-10-31
Participants
Target number of participants: 268
Treatments
No_intervention: Waitlist control
Patients allocated to the Waitlist arm will continue receiving their usual care without any additional intervention until they have completed the outcome assessment at 24 weeks.
Experimental: Intervention group
A coaching context to enhance the well-being of individuals and to facilitate the achievement of their health-related goals. The coach will negotiate and set personalized health goals with participants, ensuring the goals are realistic, achievable, and aligned with their needs.
Related Therapeutic Areas
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov