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Nursing Intervention for Adaptation After Myocardial Revascularization

Preliminary Effectiveness of a Nursing Intervention Aimed at Improving Adaptation in Patients and Their Caregivers During the Outpatient Postoperative Period Following Myocardial Revascularization

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07576569
Acronym
ADAPT-CABG
Enrollment
40
Registered
2026-05-08
Start date
2027-01-01
Completion date
2027-12-01
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Myocardial Revascularization, Nursing Care, Postoperative Recovery After Cardiac Surgery

Keywords

Myocardial Revascularization, Nursing Intervention, Patient-Caregiver Dyad, Adaptation, Postoperative Recovery, Cardiovascular Disease, Randomized Controlled Trial, Outpatient Care

Brief summary

Introduction: Myocardial revascularization is an essential procedure for patients with cardiovascular disease. Its recovery in the outpatient setting involves significant challenges for both the patient and the caregiver. This recovery phase may generate physical, emotional, and psychological complications that require an effective adaptation process of the patient-caregiver dyad to ensure successful recovery and improved quality of life. Objective: To evaluate the preliminary effectiveness of a nursing intervention aimed at improving adaptation in the patient-caregiver dyad during the outpatient postoperative period following myocardial revascularization, compared with usual care, in Bucaramanga during the period 2026-2027. Materials and Methods: A pilot randomized controlled trial will be conducted to develop and evaluate a novel nursing intervention aimed at promoting adaptation in patients undergoing outpatient postoperative myocardial revascularization and their caregivers. The intervention will be designed and its feasibility, acceptability, and preliminary effectiveness will be assessed. Data analysis will be performed using descriptive and inferential statistical methods, considering the distribution and behavior of the data. Expected Results: The study is expected to assess the preliminary effectiveness of the proposed intervention through the integration of theoretical and empirical components.

Interventions

Structured nursing intervention focused on improving adaptation in the patient-caregiver dyad through education, emotional support, and follow-up care.

OTHERUsual Care

Participants will receive standard postoperative care without the structured nursing intervention.

Sponsors

Universidad de la Sabana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Participants (patients and caregivers) will be blinded to group allocation and will not be informed whether they are receiving the structured nursing intervention or usual care. Outcome assessors will also be blinded to group assignment to reduce assessment bias. Due to the nature of the intervention, care providers and investigators cannot be blinded.

Intervention model description

Participants will be randomly assigned to one of two parallel groups: an experimental group receiving a structured nursing intervention and a control group receiving usual care. The intervention will be delivered over a 30-day outpatient postoperative period following myocardial revascularization. Outcomes will be assessed at baseline and after the intervention period to compare effectiveness between groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Adaptation level in the patient-caregiver dyadBaseline and 30 days post-dischargeAdaptation will be assessed using validated instruments that measure dimensions related to the Roy Adaptation Model, including physiological, self-concept, role function, and interdependence domains in both patient and caregiver.

Countries

Colombia

Contacts

CONTACTDébora Milena Alvarez Yañez, PhD(c)
deboraalya@unisabana.edu.co+57 3112323289
CONTACTGloria Carvajal Carrascal, PhD
gloria.carvajal@unisabana.edu.co+57 3115062590
PRINCIPAL_INVESTIGATORAlvarez Yañez

Universidad de la Sabana

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026