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Acceptance-based Healthy Lifestyles Program for Patients With Pneumoconiosis

Not Applicable
Not yet recruiting
Conditions
Healthy Lifestyle
Pneumoconiosis
Interventions
Other: Acceptance-based healthy lifestyles program (control group)
Other: Acceptance-based healthy lifestyles program (intervention group)
Registration Number
NCT06563674
Lead Sponsor
Chinese University of Hong Kong
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  1. Ethnic Chinese who is able read and speak Chinese.
  2. Adults aged 18 or over.
  3. Taking compensation for pneumoconiosis.
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Exclusion Criteria
  1. Those who have mental, visual, hearing, or cognitive impairments with regular medical follow-ups and treatment.
  2. Those who are unable to give written consent.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
ControlAcceptance-based healthy lifestyles program (control group)Participants will receive the acceptance-based healthy lifestyles program between week 8-14.
InterventionAcceptance-based healthy lifestyles program (intervention group)Participants will receive the acceptance-based healthy lifestyles program between week 1-6.
Primary Outcome Measures
NameTimeMethod
Psychological flexibilityBaseline, week 6, and week 14

Measured by Acceptance and Action Questionnaire-II Chinese version. It is a 7-point Likert scale with 7 items. The score ranges from 7 to 49 and a higher total score indicates less flexibility.

Secondary Outcome Measures
NameTimeMethod
Exercise-related outcomeBaseline, week 6, and week 14

Measured by Self-Efficacy for Exercise scale Chinese version The Chinese scale has 9 items, 11-point Likert scale. A higher total score indicates people have more self-efficacy to do exercise, range from 0 to 90.

Blood pressureBaseline, week 6, and week 14

Measured by validated and reliable upper-arm automated system after resting for 20 min

Practice of healthy dietBaseline, week 6, and week 14

Measured by the diet subscale of the Chinese version of Health Promoting Lifestyle Profile II The subscale consists of 8 items to assess the practice of healthy diet. It is a 4-point Likert scale that a higher score indicates the more practice of healthy diet (range 8 to 32).

Body weightBaseline, week 6, and week 14

Measured by a calibrated digital body monitor with participants wearing similar light clothing without shoes and socks

Waist circumferenceBaseline, week 6, and week 14

Measured in nearest 0.1 centimeter

Glycated hemoglobin (HbA1c)Baseline and week 14

blood test

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