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Evaluating the Effectiveness of an Early Exercise Program After Breast Reconstruction

Randomized Controlled Study to Evaluate the Effect of Early Exercise on Functional Restoration of Exercise and Surgical Outcomes After Breast Reconstruction

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06552650
Enrollment
72
Registered
2024-08-14
Start date
2023-11-20
Completion date
2025-06-30
Last updated
2024-08-14

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

Conditions

Braest Cancer, Breast Reconstruction

Brief summary

Breast reconstruction is an important step and option after mastectomy and can help improve the quality of life of breast cancer patients. Therefore, the proportion of patients undergoing breast reconstruction in conjunction with mastectomy is steadily increasing. Despite recent advances in less invasive techniques, postoperative movement restrictions are unavoidable, and these postoperative pain or functional limitations can last for months to years. Patients most often experience a decrease in shoulder function, which negatively impacts their physical function and is an important factor in their ability to perform activities of daily living. Early postoperative exercise has been proven to have positive results in promoting the recovery of shoulder function in breast cancer patient. However, there is a lack of research on the effectiveness of early postoperative exercise in the context of breast reconstruction. Therefore, this study aims to evaluate the effect of early postoperative exercise on patients' shoulder and trunk function after breast reconstruction.

Interventions

BEHAVIORALExercise

Four supervised exercise interventions after surgery: One exercise education session per week from postoperative day 5 through 1 month Subsequent home-based exercise: Home-based exercise recommendations from 1 month to 3 months post-surgery

OTHERUsual Care

The full spectrum of patient care practices in which clinicians have the opportunity (which is not necessarily seized) to individualize care

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Adult women between the ages of 19 and 70 2. Pathologically diagnosed with breast cancer 3. Scheduled to undergo unilateral or bilateral mastectomy and breast reconstruction

Exclusion criteria

1. Adult women age 70 and order who have been diagnosed with breast cancer 2. Had surgery or radiation therapy to the same side of the armpit 3. Scheduled to undergo or have undergone delyed breast reconstruction 4. Have breast cancer that has spread to other cancers or is metastatic 5. Deemed by the healthcare provider to have unmeasurable postoperative complications (seroma, laceration, lymphedema observed within 1 month of surgery) 6. Have problems reading or understanding Korean or have problems communicating with the researcher 7. Have difficulty exercising as judged by the healthcare provider

Design outcomes

Primary

MeasureTime frameDescription
Shoulder Range of Motion1 Day before surgery, 5 Days after Surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryShoulder Range of Motion: Objectively measures shoulder range of motion (in degree) and measurements include shoulder flexion, abduction, internal rotation, external rotation and extension.
Shoulder Strength1 Day before surgery, 5 Days after Surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryShoulder Strength: Objectively measures shoulder strength (in newton) and measurements include shoulder flexion, abduction, internal rotation, external rotation and extension.
Trunk Range of Motion1 Day before surgery, 5 Days after Surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryTrunk Range of Motion: Objectively measures trunk extension range of motion (in degree).
Trunk Strength1 Day before surgery, 5 Days after Surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryTrunk Strength: Objectively measures trunk flexion strength (in newton).

Secondary

MeasureTime frameDescription
Shoulder Pain and Disability1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryDASH (Disabilities of the Arm, Shoulder, and Hand) questionnaires) questionnaires will be administered to asses shoulder pain and disability. Minimum value of 0, maximum value of 100, with higher scores indicating greater dysfunction
Weight1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryWeight (in kilograms) will be measured with InBody
Postoperative Satisfaction after Breast reconstruction1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryPostoperative Satisfaction after Breast reconstruction: BREAST-Q questionnaires will be administered to assess postoperative satisfaction (satisfaction with breast, psychosocial well-being, and sexual well-being). Minimum value of 0 and a maximum value of 100, with higher scores indicating greater satisfaction.
BMI1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryBMI (in kg/m²) will be measured with InBody
Body fat1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryBody fat (in percentage) will be measured with InBody
Muscle mass1 Day before surgery, 10-14 Days after surgery, 1 Month after surgery, 3 Months after surgery, 6 Months after surgeryMuscle mass (in kilograms) will be measured with InBody

Countries

South Korea

Contacts

Primary ContactDong Won Lee
XYPHOSS@yuhs.ac82-2228-2215

Outcome results

None listed

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