The Development of a Gamified Web-based Pain Management Program (GAP) for Community-dwelling Older Adults With Chronic Pain

Chronic Pain Syndrome Clinical Trial

Official title:

The Development of a Gamified Web-based Pain Management Program (GAP) for Community-dwelling Older Adults With Chronic Pain

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06387706
• Other study ID #: GAP
• Status: Recruiting
• Phase: N/A
• Start date: December 1, 2023
• Est. completion date: November 30, 2024

Study information

• Verified date: April 2024
• Source: The Hong Kong Polytechnic University
• Contact: Mimi Mun Yee Tse, PhD.
• Phone: 39708764
• Email: mmytse[@]hkmu.edu.hk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Pain Management in Older Adults: Pain significantly impacts the well-being of older adults, often leading to diminished physical abilities and a reduced quality of life. Despite this, pain management remains suboptimal, with concerns about medication side effects and a tendency to view pain as a natural aspect of aging. Consequently, many seniors are hesitant to use painkillers. As an alternative, non-pharmacological strategies such as educational programs, physical activity, massage, relaxation techniques, and music therapy are gaining traction.

Innovative Non-Drug Solutions: To improve participation in non-medication pain relief methods, we suggest incorporating gaming elements into these programs (GAP). Originating in digital media in 2008, gamification has since spread across various industries. It involves adding game-like elements to activities to boost engagement, experience, and motivation.

Project Goals: The aims of this initiative include creating a web-based Gamified Pain Management Program (GAP), engaging older adults with chronic pain in the development of GAP, and gathering their feedback on the program's effectiveness.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 4
• Est. completion date: November 30, 2024
• Est. primary completion date: July 30, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• Aged 60 or above

• Can understand Cantonese

• Scored >6 in the Abbreviated Mental Test; a cut-off point of 6 is valid for differentiating between normal and abnormal cognitive functions in geriatric clients

• Have a history of non-cancer pain in the past 6 months

• Have a pain score of at least 2 on the Numeric Rating Scale

• Able to take part in light exercise and stretching

• Owns a smartphone and can access the Internet

Exclusion Criteria:

• Have severe visual and/or auditory deficits that affect that seeing and hearing

• Have a serious organic disease or malignant tumor

• Have a mental disorder diagnosed by neurologists or psychiatrists

• Had a surgical treatment in the past two months

• Experienced drug addiction

Related Conditions & MeSH terms

• Chronic Pain
• Chronic Pain Syndrome

Intervention

Other:
• Gamified web-based pain management Program
Gamified Program Development: The project aims to create a Gamified web-based pain management Program (GAP) tailored for older adults with chronic pain, enhancing engagement through gaming elements. Inclusive Design Process: Older adults with chronic pain will actively participate in developing GAP, providing valuable feedback throughout the process. Pilot Study Design: A pre and post study design will be employed, with a small pilot group of 4 participants to offer diverse perspectives in the program's development. Educational Content & Activities: GAP will feature interactive educational content on pain effects, medication, non-drug treatments, and exercises, delivered through a mobile-friendly web platform.

Locations

Country	Name	City	State
Hong Kong	Hong Kong Metropolitan University	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain Relief	Conducting pre- and post-test of Brief Pain Inventory	4-week