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Study identifier: NCT07649330 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effects of Myofascial Release on Cardiac Patients After Median Sternotomy

Condition: Aortic Aneurysm and Dissection · Coronary Artery Disease (CAD) · Valve Heart Disease  ·  Sponsor: Siou-Pin Huang

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

After deciding to join this study and signing the informed consent form, participants will undergo the following interventions: All participants will receive a preoperative assessment (Tp) before surgery. Within five days after transferring from the ICU to the general ward, participants will receive a baseline assessment (T0). After completing seven sessions of myofascial release (MFR), a post-intervention assessment (T1) will be conducted. Assessments include maximum inspiratory pressure (MIP), maximum expiratory pressure (MEP), pulmonary function tests, mid- and lower-thoracic mobility, surface electromyography (sEMG) to measure diaphragmatic and sternocleidomastoid muscle activity, and pain scores. Pulmonary function tests include forced vital capacity (FVC), forced expiratory volume in one second (FEV1), FEV1/FVC ratio, and maximum voluntary ventilation (MVV). Participants will be randomly assigned to an intervention group or a control group. The intervention group will receive myofascial release therapy in addition to routine physical therapy in the general ward. Routine therapy includes daily physical therapy sessions such as out-of-bed activities, incentive spirometry training (Triflow), and functional exercises. The MFR intervention consists of three steps: The therapist places both hands on the thoracic outlet, with the index and middle fingers above the clavicle. One hand is placed on the anterior chest and the other hand parallel on the participant's back. Bo…

This description comes directly from the study's public registry record.

Talk to the study team

Siou Pin Huang, PT (Physical Therapist)  ·  +886 988 366 335  ·  qaz9650921@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Kaohsiung Veterans General HospitalKaohsiung City, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT07649330