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Telerehabilitation vs. Center-Based Rehab for Psychological Well-being After CABG

The Impact of Home-Based Telerehabilitation Versus Center-Based Cardiac Rehabilitation on Anxiety, Depression, and Quality of Life After Coronary Artery Bypass Grafting: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07232693
Enrollment
110
Registered
2025-11-18
Start date
2024-06-01
Completion date
2025-08-01
Last updated
2025-11-18

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

Conditions

Psychological Distress After Coronary Artery Bypass Grafting (CABG)

Keywords

Coronary Artery Bypass Grafting, Telerehabilitation, Anxiety, Depression, Quality of Life, Cardiac Rehabilitation

Brief summary

This randomized controlled trial aims to determine if a 12-week home-based telerehabilitation (HBTCR) program is as effective as traditional center-based cardiac rehabilitation (CBCR) in improving psychological well-being (anxiety and depression) and quality of life in patients who have undergone coronary artery bypass grafting (CABG). A third group receiving usual care served as a control.

Detailed description

Psychological distress, such as anxiety and depression, is common after coronary artery bypass grafting (CABG) and negatively affects recovery and quality of life. While center-based cardiac rehabilitation (CBCR) effectively addresses these issues, participation is often limited by barriers like travel, cost, and scheduling. Home-based telerehabilitation (HBTCR) offers a potential solution. This single-center, prospective, three-arm randomized controlled trial was designed to compare the effectiveness of HBTCR versus CBCR and usual care. A total of 110 clinically stable patients, 4-8 weeks post-CABG, were randomly assigned in a 1:1:1 ratio to an HBTCR group, a CBCR group, or a control group. The intervention period was 12 weeks. The study hypothesized that the HBTCR program, which includes a personalized exercise plan, remote monitoring via a wearable device and mobile app, and weekly psychosocial support from a nurse, would be as effective as the traditional supervised in-person CBCR program in reducing symptoms of anxiety and depression and improving health-related quality of life.

Interventions

BEHAVIORALHome-Based Telerehabilitation Cardiac Rehabilitation

A 12-week structured and remotely monitored cardiac rehabilitation program including a personalized exercise prescription (aerobic and resistance training), remote monitoring with a wearable heart rate sensor and mobile app, and weekly one-on-one psychosocial support and counseling via phone or video call from a rehabilitation nurse.

BEHAVIORALUsual Care

Standard postoperative care including prescribed medications and routine follow-up, supplemented with health education pamphlets on lifestyle modification. No structured or supervised rehabilitation was provided.

Sponsors

The First Hospital of Hebei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Aged 30-75 years. * 4-8 weeks post-Coronary Artery Bypass Grafting (CABG). * In clinically stable condition. * Had access to a smartphone and were willing to use it for the program. * Willing to participate in a 12-week rehabilitation program. * Provided written informed consent.

Exclusion criteria

* Presence of severe and unstable comorbidities (e.g., uncontrolled heart failure, recent stroke). * Severe orthopedic limitations that would prevent participation in exercise. * Significant cognitive impairment or psychiatric disorders that would interfere with participation. * Inability to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Change in Anxiety SymptomsBaseline, 12 WeeksThe change from baseline in the Hamilton Anxiety Scale (HAMA) score. The HAMA scale is a clinician-rated scale where higher scores indicate greater symptom severity.
Change in Depression SymptomsBaseline, 12 WeeksThe change from baseline in the 17-item Hamilton Depression Scale (HAMD) score. The HAMD is a clinician-rated scale where higher scores indicate greater symptom severity.

Secondary

MeasureTime frameDescription
Change in Health-Related Quality of LifeBaseline, 12 WeeksThe change from baseline in scores on the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36). The SF-36 assesses eight domains: Physical Functioning (PF), Role-Physical (RP), Bodily Pain (BP), General Health (GH), Vitality (VT), Social Functioning (SF), Role-Emotional (RE), and Mental Health (MH). Scores for each domain range from 0 to 100, with higher scores indicating better quality of life.

Other

MeasureTime frameDescription
Change in 6-Minute Walk Distance (6MWD)Baseline, 12 WeeksThe change from baseline in the distance a patient can walk in six minutes, measuring functional exercise capacity. Unit: Meters.
Adherence RateThrough study completion, 12 weeksThe percentage of completed cardiac rehabilitation sessions out of the total prescribed sessions for the HBTCR and CBCR groups.
Change in Peak Oxygen Consumption (VO₂ peak)Baseline, 12 WeeksThe change from baseline in VO₂ peak, a measure of cardiopulmonary fitness, assessed via an exercise test. Unit: mL/kg/min.
Change in Left Ventricular Ejection Fraction (LVEF)Baseline, 12 WeeksThe change from baseline in LVEF, assessed by echocardiography. Unit: Percentage (%).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 27, 2026