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Efficacy of An Online Gamified Pain Management Programme for Adults with Chronic Pain in Mainland China: A Randomized Controlled Trial

Efficacy of An Online Gamified Pain Management Programme for Adults with Chronic Pain in Mainland China: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121536
Enrollment
Unknown
Registered
2026-03-31
Start date
2026-03-31
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic pain

Interventions

Experimental group: Online Gamified pain management (GPM):The GPM intervention is an open for 10-week program, designed as escape room game by incorporating gamification elements, educational informat
Control group:In control group, participants will receive a digital pain management resource package for a 10-week period with same components as the GPM group but delivered in a non-gamified, standar

Sponsors

Hong Kong Metropolitan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to No maximum

Inclusion criteria

Inclusion criteria: To be eligible to participate in the study, the participants must meet all the inclusion criteria: 1.aged older than 18 years old; 2.able to read and understand the Mandarin Chinese language; 3.owners of smartphones with internet access; 4.have a previously diagnosed chronic non-cancer pain condition lasting more than three months; 5.report a score of >=2 on the VAS scale.

Exclusion criteria

Exclusion criteria: The participants will be excluded if they meet one or more of the following exclusion criteria: 1.Patients with associated pathologies that make it impossible to perform physical exercise (myopathies, neurological diseases, cardiac disease, pregnancy, pulmonary diseases, infection and fracture); 2.Individuals undergoing surgery or invasive treatments in the last three months; 3.Concurrent participation (or participation within the preceding 3 months) in a supervised exercise programme or multidisciplinary treatment.

Design outcomes

Primary

MeasureTime frame
Pain intensity and interference;

Secondary

MeasureTime frame
Fear of pain;Pain Catastrophizing;Exercise adherence;Depression;Anxiety;Quality of life;User satisfaction on the games;Psychological Needs Satisfaction:;Perceptions, attitudes and experiences of the intervention;Intra-intervention variables;

Countries

China

Contacts

Public ContactMimi Mun Yee Tse

School of Nursing and Health Sciences, Hong Kong Metropolitan University

mmytse@hkmu.edu.hk+852 3970 8764

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026