Can extra nurse support boost recovery after heart bypass?
NCT ID NCT07576569
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether a structured nursing program—including education, emotional support, and follow-up calls—can help heart bypass patients and their caregivers adapt better during recovery at home. About 40 adults who recently had heart surgery and their primary caregivers will be randomly assigned to receive either the extra nursing support or usual care. The goal is to see if the program improves how well patients and caregivers cope physically and emotionally.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- structured nursing intervention (education, emotional support, follow-up care)
- What this could lead to
- If it works, this could point toward a simple, low-cost way to help heart surgery patients and their caregivers recover better at home.
- What could go wrong
- This is a very small pilot study with only 40 people, so results may not apply to everyone. It tests a behavioral program, not a drug, so any benefit is likely modest.
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 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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 years and older
- 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: * Adults aged 18 years or older who have undergone myocardial revascularization surgery, completed the immediate postoperative in-hospital period without major complications, and have been discharged for outpatient management according to institutional protocols * Patients who, at the time of discharge, do not require ventilatory support, invasive hemodynamic support, or continuous monitoring, and present documented clinical stability * Presence of an identified primary caregiver actively involved in the home care process during the outpatient postoperative period * Preserved cognitive capacity in both patient and caregiver, allowing understanding of instructions, participation in the intervention, and completion of assessment instruments * Written informed consent provided by both patient and caregiver Exclusion Criteria: * Patients presenting severe postoperative complications, such as deep surgical site infection, persistent hemodynamic instability, major neurological events, or readmission to the intensive care unit at the start of the intervention Patients with moderate to severe cognitive impairment, decompensated psychiatric disorders, or neurological conditions that limit understanding, communication, or active participation * Caregivers with physical, cognitive, or emotional limitations that compromise the effective performance of the caregiving role during the follow-up period * Patients without a clearly identified support network or without an available primary caregiver to participate in the study * Concurrent participation in other clinical, educational, or psychosocial intervention studies that may interfere with the proposed intervention * Language or cultural barriers that prevent understanding of the intervention content or interaction with the research team, without adequate mediation
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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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Universidad de La Sabana
Bogotá, Bogota D.C., 250001, Colombia
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