Home based cardiac rehabilitation
Behavioral12 week home based cardiac rehabilitation include Physical exercise, dietary management, smoking cessation and stress management
NCT Number: NCT06625463
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
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Not applicable
Gadjah Mada University, Sleman, Special Region of Yogyakarta, Indonesia
How to enroll patients as research subjects Inpatients
Outpatients
Intervention HBCR with FCEM approach
During the intervention period, the family reported daily diets, medication adherence and exercise activities as well as HR during exercise through a daily google form that would be monitored by the facilitating nurse.
The control group will receive education on the components of medication adherence, exercise, smoking behaviour, diet, and stress management for 1 session.
Forms of protection for patients and families:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
>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.
Exclusion criteria
12 week home based cardiac rehabilitation include Physical exercise, dietary management, smoking cessation and stress management
Time frame: From enrollment to the end of treatment at 12 weeks
Individuals perception of their level of health, current condition which includes physical, psychological and social dimensions, will be measured with MacNew Heart questionnaire. scored from 1 (low HRQOL) to 7 (high HRQOL). The maximum possible score in any domain is 7
Time frame: From enrollment to the end of treatment at 12 weeks
peak vo2 achieved based on 6minute walk test, in ml/kg/min
Contact information is provided by the study sponsor or research team.
Gadjah Mada University
Other
Acronym: HBCR in ACS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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