Balikesir Ataturk City Hospital Affiliated with University of Health Sciences
Balıkesir, Turkey (Türkiye)
NCT Number: NCT07240584
This prospective prehabilitation trial evaluated the effectiveness of an individualized exercise program initiated before breast cancer surgery and maintained for 12 months. The intervention aimed to promote functional recovery and improve patient-reported outcomes.
Looking for future studies?
Notify Me18 year and older
Female
Interventional
Not applicable
Balıkesir, Turkey (Türkiye)
Women scheduled for breast surgery due to breast cancer were enrolled in an individualized prehabilitation program that began in the preoperative period and continued for 12 months. The exercise program included range-of-motion, strengthening, and postural correction exercises delivered through supervised and home-based sessions. Outcomes were evaluated at baseline and at 1st, 3rd, 6th, and 12th months. Functional outcomes, shoulder range of motion, pain intensity, lymphedema development, and patient-reported quality of life were assessed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The exercise program was delivered to patients through both visual and written materials, accompanied by face-to-face training sessions conducted by a physiotherapist. A home-based program was designed separately for the pre-surgery phase, postoperative day 1, day 3, day 7, and the maintenance period.
The exercise template included postural correction, breathing, aerobic, stretching, and resistive strengthening exercises targeting muscles in adjacent to the shoulder joint and mobilization of scapulothoracic complex via stretching and strengthening exercises of periscapular muscles.
Time frame: baseline, 1st-3rd-6th-12th month
Measurement of Flexion, Abduction, Internal and External Rotation of Shoulder with goniometer
Time frame: baseline, 1st-3rd-6th-12th month
measure of pain with VAS (Visual analog scale)
Time frame: baseline and 12th month
measure of upper extremity functions with UEFI-15 (Upper extremity functional index) instrument
Time frame: baseline and 12th month
measure of fatigue condition with FSS (Fatigue severity scale) instrument
Time frame: baseline and 12th month
measure of Quality of Life with EORTC-QLQ-C30 (European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire) instrument
Time frame: baseline and 12th month
Limb volume difference >10% or clinical signs of edema
University of Health Sciences Balikesir Hospital Eduation and Research
Other Gov
The Impact of Exercise Prehabilitation on Upper Extremity Range of Motions, Functionality and Quality of Life in Breast Cancer Survivors: A Prospective Clinical Trial
Acronym: Prehab of BC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03194997
Behavior, Behavioral Symptoms
Florianópolis, Santa Catarina, Brazil
View Trial DetailsNCT00027118
Breast Cancer, Breast Diseases
Bethesda, Maryland, United States
View Trial DetailsNCT00679185
Breast Cancer, Breast Diseases
Nashville, Tennessee, United States
View Trial DetailsNCT04401189
Behavior, Behavioral Symptoms
Aarhus, Denmark
View Trial Details