Breast Neoplasms Clinical Trial
Official title:
Post-mastectomy Women Underwent Transverse Rectus Abdominis Musculocutaneous Flap (TRAM) Surgery: Its Influence on Abdominal Muscle Function and the Effects of Therapeutic Exercises
| Verified date | February 2021 |
| Source | Kaohsiung Medical University Chung-Ho Memorial Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The unilateral transverse rectus abdominis musculocutaneous (TRAM) flap is a major operation widely used for breast reconstruction. It is hypothesized that this surgery has the potential risk of weakening the abdominal wall because it disrupts the integrity of the rectus abdominis muscle (RA), therefore, alters the insertion of the oblique muscles and the biomechanical relationship between the RA muscle and adjacent structures. The purposes of this study were to examine the effects of the TRAM flap surgery on muscle size of abdominal muscles, strength and endurance of trunk muscles, strength and endurance of core stability, as well as the effects of therapeutic exercises on it in post-mastectomy women underwent TRAM surgery.
| Status | Completed |
| Enrollment | 82 |
| Est. completion date | September 8, 2014 |
| Est. primary completion date | September 8, 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Female |
| Age group | 30 Years to 60 Years |
| Eligibility | Inclusion Criteria: 1. Healthy adults - Their age should be ranged between 30 - 60 years 2. TRAM flap surgery patients - at least 6 months after the MS pedicled TRAM flap surgery Exclusion Criteria: 1. Healthy adults - a history of injury resulting in an inability to perform activities of daily living - scoliosis or spinal surgery - neurological, neuromuscular, rheumatological or systemic diseases 2. TRAM flap surgery patients - tumor distant metastasis - a history of injury resulting in an inability to perform activities of daily living - scoliosis or spinal surgery - neurological, neuromuscular, rheumatological or systemic diseases |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Kaohsiung Medical University Chung-Ho Memorial Hospital |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Changes in thickness of abdominal wall muscles at 12-week | Using the Ultrasound imaging to measure the thickness of all abdominal wall muscles at rest and in an isometric contraction. | The assessments will be conducted 1 and 12 weeks following the intervention | |
| Primary | Changes in the cross-sectional area of the rectus abdominis muscle (RA) muscle at 12-week | Using the Ultrasound imaging to measure the cross-sectional area of the rectus abdominis muscle at rest and in an isometric contraction. | The assessments will be conducted 1 and 12 weeks following the intervention | |
| Primary | Changes in strength of the trunk muscles at 12-week | Using the dynamometer and clinical tests (prone extension, curl-up and rotational curl-up) to measure the trunk strength | The assessments will be conducted 1 and 12 weeks following the intervention | |
| Primary | Changes in endurance of the trunk muscles at 12-week | Using the clinical tests (abdominal muscle test for strength, unsupported double bend leg lifting for static endurance) to measure the endurance of trunk muscles | The assessments will be conducted 1 and 12 weeks following the intervention | |
| Primary | Changes in balanced functions at 12-week | Using the seconds in the following static position to measure the balance: one-leg standing with the other lift-leg 1 inch of ground clearance; single leg standing with the other lift-leg hip flexion 90 degrees and the tibia vertical to the floor. | The assessments will be conducted 1 and 12 weeks following the intervention | |
| Primary | Changes in muscle activity of selected trunk and limb muscles at 12-week | Using A six-camera Qualisys motion system to measure the muscle activity of selected trunk and limb muscles. | The assessments will be conducted 1 and 12 weeks following the intervention |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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