NCT07762898Not yet recruiting
Sedentary Behavior Intervention for Older Adults With Coronary Heart Disease and Frailty
Development and Application of a Sedentary Behavior Intervention Program Based on the Integrated Theory of Health Behavior Change for Older Adults With Coronary Heart Disease and Frailty
Source: ClinicalTrials.gov · Last updated 13 Aug 2026
Brief summary (registry, in English)
This study aims to evaluate the feasibility and effectiveness of a sedentary behavior intervention based on the Integrated Theory of Health Behavior Change (ITHBC) in older adults with coronary heart disease and frailty. Participants will be randomly assigned to an intervention group or a control group. The intervention is designed around the three core components of ITHBC-knowledge and beliefs, self-regulation skills and abilities, and social facilitation-to help participants reduce sedentary behavior, improve physical activity, and enhance their ability to manage health-related behaviors. The study will include a 1-month intervention period followed by a 2-month follow-up period, with a total study duration of 3 months for each participant. Changes in sedentary behavior and other health-related outcomes will be assessed throughout the study period.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 64 (estimated)
- First submitted
- 10 Aug 2026
- Start date
- 1 Sept 2026
- Primary completion date
- 31 Jan 2027
- Lead sponsor
- Gansu University of Chinese Medicine
- Diseases
- Coronary artery disease
- NCT number
- NCT07762898
What you commit to
- Study type: Interventional
- Planned participants: 64
- From 1 Sept 2026 to the primary completion date, 31 Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Presence of a malignant tumor.
- Presence of a severe infectious disease.
- Presence of a physical impairment that substantially limits limb mobility.
- Presence of a language impairment that prevents effective communication or -completion of study assessments.
- Presence of cognitive impairment that prevents understanding of study procedures or completion of study assessments.
Other
- Currently participating in another research study.
Who the study is looking for
- Age 60 years or older.
- Diagnosis of stable coronary artery disease according to the Chinese Primary -Care Guideline for Stable Coronary Artery Disease (2020).
- Canadian Cardiovascular Society (CCS) angina class I or II.
- Fried Frailty Phenotype score of 1 or higher, including participants with pre-frailty (score 1-2) or frailty (score 3-5).
- Total sedentary time of 6 hours or more per day.
- The participant or the participant's primary caregiver is able to use the WeChat application.
- Able and willing to provide informed consent and voluntarily participate in the study.
Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Affiliated Hospital of Gansu University of Chinese Medicine Coordinator of this site? Confirm its status | Lanzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.