A tailored coaching plan may keep heart patients on track after hospital discharge
NCT ID NCT07799376
First seen Sep 02, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This trial tests a 'Hospital-to-Home' support program for people recovering from acute coronary syndrome, a group of heart emergencies like heart attacks. Participants are randomly assigned to either the structured program or standard education. The program uses behavior change models to tailor coaching based on each patient's readiness and personal barriers. Researchers compare self-management skills and heart health outcomes between the two groups over 60 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A structured self-management support program based on the COM-B and HAPA behavior change models
- What this could lead to
- If it works, this program could help ACS patients stick to heart-healthy habits after discharge, potentially reducing repeat heart events and improving quality of life.
- What could go wrong
- This is a small, early-stage trial with 80 participants, so results may not apply to everyone. The program relies on patient motivation and WeChat use, which may limit its reach.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosed with acute coronary syndrome (ACS) according to the Guidelines for the Rapid Emergency Diagnosis and Treatment of Acute Coronary Syndrome (2019), based on electrocardiogram (ECG), serological tests, and symptomatology. * Age ≥ 18 years. * Mentally alert, with unimpaired communication skills, and adequate reading and expressive abilities. * Patient, or their primary caregiver, able to use the study communication tool (WeChat). Exclusion Criteria: * Advanced or terminal stage of disease with expected survival less than 12 months. * Severe physical comorbidities (e.g., decompensated cardiac, hepatic, or renal function). * Motor dysfunction or mobility impairment. * Currently participating in or previously participated in a similar clinical study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Nanfang Hospital, Southern Medical University
Guangzhou, Guangdong, 510515, China
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