Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06563674

Acceptance-based Healthy Lifestyles Program for Patients With Pneumoconiosis

Led by Chinese University of Hong Kong · Updated on 2025-04-13

80

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Symptoms, such as cough and shortness of breath, are common among patients with pneumoconiosis. Depression and anxiety can be elicited by the symptoms, while avoidance of daily activities is believed to reduce trigger of symptoms. The lung function is then declined and the risk of having stroke and heart failure is increased. The objectives of this 2-arm waitlist pilot randomized controlled trial are to test the effects and feasibility of an acceptance-based educational program among patients with pneumoconiosis. 80 participants will be recruited from community centers and randomly assigned to intervention group or waitlist-control group in a ratio of 1:1. The 6-week group-based educational program will be provided to the intervention group first, then the waitlist-control group. The program consists of 4 sessions integrated with acceptance components and care of pneumoconiosis. Their psychological health, healthy lifestyles, and cardiometabolic profiles will be assessed at baseline, week 6, and week 14. Data will be analyzed using a statistical package. The feasibility of the program will be evaluated by interview. The findings of this study can inform the integration of acceptance-based intervention into pneumoconiosis management in Hong Kong, and future study on chronic progressive lung diseases.

CONDITIONS

Official Title

Acceptance-based Healthy Lifestyles Program for Patients With Pneumoconiosis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ethnic Chinese who can read and speak Chinese
  • Adults aged 18 years or older
  • Currently receiving compensation for pneumoconiosis
Not Eligible

You will not qualify if you...

  • Having mental, visual, hearing, or cognitive impairments requiring regular medical follow-ups and treatment
  • Unable to provide written consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

PMAA

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

H

Hon Lon Tam, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

OTHER

Number of Arms

2

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