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Empowering Sustainable Therapeutic Engagement with Music (ESTEEM): A Pilot Study of a Self-administered Music Therapy Program for Cardiac Rehabilitation Participants in Thailand

Not Applicable
Recruiting
Conditions
Depression in cardiac rehabilitation participants
Anxiety in cardiac rehabilitation participants
Stress in cardiac rehabilitation participants
Cardiovascular - Coronary heart disease
Cardiovascular - Other cardiovascular diseases
Mental Health - Anxiety
Mental Health - Depression
Registration Number
ACTRN12623000009617
Lead Sponsor
The University of Melbourne
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
24
Inclusion Criteria

The participants will be recruited from the research site (i.e., a hospital cardiac rehabilitation unit in Bangkok, Thailand). The inclusion criteria are 1) adult participants in Phase 2-3 of the cardiac rehabilitation program of the research site hospital, 2) clinically stable and showing evidence of expected physical recovery, 3) physically independent, 4) intact cognitive functioning, 5) functional visual/hearing with or without aids, 6) fluent in Thai, 7) able to conveniently travel to the hospital for sessions and data collection, 8) express interest in using music to promote psychological wellbeing and willing to participate throughout the course of the study, and 9) consent to participate in the study and able to make consent independently.

Exclusion Criteria

The participants will be excluded if 1) have other health conditions that could be obstacles to participation (such as cognitive, sensory, or communication impairment, and uncontrolled health conditions), 2) have a history of psychiatric or neurological disorder that impedes their capacity to participate in the intervention, 3) have uncontrolled life-threatening condition, 4) participate in a concurrent research study and/or another lifestyle changing program other than cardiac rehabilitation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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