NCT06625463 Development and Implementation Model of Home Based Cardiac Rehabilitation With Family Empowerment Approach in Patient With ACS (HBCR in ACS)
| NCT ID | NCT06625463 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Gadjah Mada University |
| Condition | Home Based Rehabilitation |
| Study Type | INTERVENTIONAL |
| Enrollment | 90 participants |
| Start Date | 2025-01-01 |
| Primary Completion | 2025-06-10 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 90 participants in total. It began in 2025-01-01 with a primary completion date of 2025-06-10.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this clinical trial is to determine whether home-based cardiac rehabilitation with a family empowerment approach can help acute coronary syndrome patients recover. The main questions to be answered are: \- Does home-based cardiac rehabilitation with a family approach effective in patients with acute coronary syndrome to improve health-related quality of life and peak Vo2? Researchers will compare with usual care to see if home-based cardiac rehabilitation with a family approach is more effective for improving health-related quality of life and peak Vo2 in ACS patients. Patient inclusion criteria 1. Patients with acute coronary syndrome who had undergone hospitalization, with a minimum home care time of 3 months and a maximum of 1 year, calculated from the day of discharge from the hospital until the time of the interview. 2. Aged 18-65 years old, participants were selected with age variations representing young adults, adults and the elderly. 3. Patients with first experience of SCA, participants were selected whether they had undergone PCI or not. 4. Patients living with family and family involved in the patient care process. 5. Physical condition allows for interviews. physical condition is evidenced by examination of stable vital signs (diastolic BP \>90, systolic \<150 mmhg; N: 60-100x/min; S: 36-380c, no pain). Psychological condition does not show symptoms of depression as measured by the Patient Health Questionnaire-9 instrument. 6. Willing to participate in the study. Participants will: For 12 weeks 1. Perform walking exercises as prescribed 2. Implement diets and stress management according to the module 3. Quit smoking 4. Medication compliance 5. visit the clinic to see a cardiologist, undergo a 6-minute walk test
Eligibility Criteria
Inclusion Criteria: 1. Patients with acute coronary syndrome who have undergone hospitalization, with a minimum home care time of 3 months and a maximum of 1 year, calculated from the day of discharge from the hospital until the time of interview. 2. Aged 18-65 years, participants were selected with age variations representing young adults, adults and the elderly. 3. Patients with first experience of SCA, participants were selected whether they had undergone PCI or not. 4. Patients living with family and family involved in the patient care process. 5. Physical condition allows for interviews. physical condition is evidenced by examination of stable vital signs (diastolic BP \>90, systolic \<150 mmhg; N: 60-100x/min; S: 36-380c, no pain). Psychological condition does not show symptoms of depression as measured by the Patient Health Questionnaire-9 instrument. 6. Willing to participate in the study. Exclusion Criteria: * Patients with comorbidities that require routine medication such as Diabetes Mellitus, hypertension, renal failure
Contact & Investigator
Anggoro Budi Hartopo, PhD
STUDY DIRECTOR
Gadjah Mada University
Frequently Asked Questions
Who can join the NCT06625463 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Home Based Rehabilitation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06625463 currently recruiting?
Yes, NCT06625463 is actively recruiting participants. Contact the research team at evamarti85@gmail.com for enrollment information.
Where is the NCT06625463 trial being conducted?
This trial is being conducted at Sleman, Indonesia, Yogyakarta, Indonesia.
Who is sponsoring the NCT06625463 clinical trial?
NCT06625463 is sponsored by Gadjah Mada University. The principal investigator is Anggoro Budi Hartopo, PhD at Gadjah Mada University. The trial plans to enroll 90 participants.