NCT07034937

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for not_applicable coronary-artery-disease

Timeline
3mo left

Started Aug 2025

Shorter than P25 for not_applicable coronary-artery-disease

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress77%
Aug 2025Jul 2026

First Submitted

Initial submission to the registry

June 9, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

June 24, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

August 1, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Expected
Last Updated

June 24, 2025

Status Verified

June 1, 2025

Enrollment Period

8 months

First QC Date

June 9, 2025

Last Update Submit

June 19, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Diaphragm Excursion (cm)

    The vertical movement of the diaphragm during the respiratory cycle shows the function and mobility of the diaphragm in the process of pulmonary ventilation. The data obtained is expressed in cm. Measured via ultrasound.

    Baseline to Week 6

Secondary Outcomes (3)

  • Forced Vital Capacity (FVC)

    Baseline to Week 6

  • Forced Expiratory Volume in one second (FEV1)

    Baseline to Week 6

  • Peak Expiratory Flow (PEF)

    Baseline to Week 6

Study Arms (1)

Aerobic and Resistance Training Group

EXPERIMENTAL
Other: Combination of aerobic training (treadmill walking) and resistance training

Interventions

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.

Aerobic and Resistance Training Group

Eligibility Criteria

Age40 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Coronary Artery Disease

Interventions

Resistance Training

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Dian M Sari, MD., M.Sc., Ph.D

    Faculty of Medicine Universitas Padjadjaran Bandung

    PRINCIPAL INVESTIGATOR

Central Study Contacts

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

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Single Group Assignment (Pretest-Posttest)
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 9, 2025

First Posted

June 24, 2025

Study Start

August 1, 2025

Primary Completion

April 1, 2026

Study Completion (Estimated)

July 30, 2026

Last Updated

June 24, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share