Aerobic and Resistance Training in Post-CABG Patients

NCT ID: NCT07034937

Last Updated: 2025-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-01

Study Completion Date

2026-07-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study investigates the effect of combined aerobic and resistance training using resistance bands on diaphragmatic excursion and pulmonary function (FVC, FEV₁, PEF) in post-CABG patients undergoing phase II cardiac rehabilitation.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This quasi-experimental study with a pretest-posttest design evaluates the impact of a 6-week structured aerobic and resistance training program using resistance bands on the diaphragm excursion and pulmonary function. Conducted at the rehabilitation polyclinics of Hasan Sadikin and Al Ihsan hospitals, this study includes post-CABG patients meeting specific inclusion criteria. Intervention is performed twice a week and includes treadmill walking and upper/lower limb resistance exercises. Outcomes will be assessed via ultrasound for diaphragm excursion and spirometry for lung function.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Coronary Artery Disease Post Coronary Artery Bypass Grafting

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single Group Assignment (Pretest-Posttest)
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Aerobic and Resistance Training Group

Group Type EXPERIMENTAL

Combination of aerobic training (treadmill walking) and resistance training

Intervention Type OTHER

Combination of aerobic training (treadmill walking) and resistance training using resistance bands for deltoid, biceps, triceps, and quadriceps muscles. Conducted twice weekly for 6 weeks (12 sessions). Tools include treadmill and theraband loop bands.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Combination of aerobic training (treadmill walking) and resistance training

Combination of aerobic training (treadmill walking) and resistance training using resistance bands for deltoid, biceps, triceps, and quadriceps muscles. Conducted twice weekly for 6 weeks (12 sessions). Tools include treadmill and theraband loop bands.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Patients post-CABG surgery maximum 12 weeks after the procedure
2. Age 40-65 years
3. Visual and hearing health
4. Ready to participate in research and sign informed consent.

Exclusion Criteria

1. Blood pressure greater than 160 mmHg for systolic and diastolic blood pressure greater than 100 mmHg
2. Patients with contraindications to aerobic and resistance training, such as fractures that limit movement.
3. Patients undergoing other therapies that may affect diaphragmatic muscle measurement results, such as electrical diaphragmatic stimulation.
Minimum Eligible Age

40 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Dr. Hasan Sadikin General Hospital, Bandung, Indonesia

UNKNOWN

Sponsor Role collaborator

Universitas Padjadjaran

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Dian M Sari, MD., M.Sc., Ph.D

Role: PRINCIPAL_INVESTIGATOR

Faculty of Medicine Universitas Padjadjaran Bandung

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Dian M. Sari, MD., M.Sc., Ph.D

Role: CONTACT

+62 812 2181 2279

Nurul Aini, MD

Role: CONTACT

+62 856 4079 0029

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IKFR-202506.01

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.