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Body Awareness, Upper Extremity Function, and Quality of Life in Breast Cancer Survivors: A Case-Control Study

Status: Recruiting
Location: See all (2) locations...
Study Type: Observational
SUMMARY

Breast cancer is one of the most common types of cancer among women and one of the leading causes of morbidity and mortality. With increasing survival rates, issues such as treatment-related morbidities and consequently upper extremity dysfunction, reduced body awareness, and decreased quality of life are frequently encountered. In the literature, the impact of treatment-related morbidities-particularly on upper extremity functions, body awareness, and quality of life-among women who have survived breast cancer treatment has not been sufficiently investigated. This gap constitutes a significant shortcoming in terms of clinical practices and the post-treatment period. This study aims to examine the effects of breast cancer treatment on upper extremity functions, body awareness, and quality of life in women who have survived breast cancer treatment, in comparison with a healthy control group. The study will be conducted at Yeditepe University Koşuyolu Hospital between May, 2025, and October, 2025. Participants will include women who have survived breast cancer treatment and a healthy control group matched based on criteria such as age and body mass index. In the study, three separate assessments will be conducted for upper extremity functions: the Quick Disabilities of the Arm, Shoulder, and Hand (QuickDASH) questionnaire for upper extremity functionality, a hand dynamometer for grip strength, and the Clinometer device for shoulder joint position sense. The Body Awareness Questionnaire will be used to assess body awareness, and the EORTC QLQ-C30 scale will be used for quality of life assessment. The IBM SPSS Statistics software package will be used for data analysis. In statistical analyses, a significance level of p\<0.05 will be considered.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 25
Maximum Age: 75
Healthy Volunteers: t
View:

• Being a woman

• Being between the ages of 25 and 75

• Having been diagnosed with Stage 0-III breast cancer

• Having completed primary treatments (surgery, chemotherapy, and/or radiation therapy) no more than 6 months prior to the assessment date

• Having received medical clearance from a physician

• Having undergone either breast-conserving surgery or mastectomy due to breast cancer

• Willingness to participate in the study voluntarily

• Being a woman

• Having a body mass index (BMI) within ±3 kg/m² of the breast cancer survivor group

• Being within ±5 years of age compared to the breast cancer survivor group

• Matching hand dominance with the breast cancer survivor group

Locations
Other Locations
Turkey
Halic University
RECRUITING
Istanbul
Yeditepe Hospital
RECRUITING
Istanbul
Contact Information
Primary
Seda Saka, PhD
sedasaka@halic.edu.tr
05447803417
Time Frame
Start Date: 2025-05-06
Estimated Completion Date: 2025-11-15
Participants
Target number of participants: 42
Treatments
Healthy control group
A group of healthy subjects, matched with the breast cancer group based on criteria such as age and body mass index, will be included in the study.
Breast cancer group
Women who have survived Stage 0-III breast cancer will be included in the study.
Related Therapeutic Areas
Sponsors
Leads: Halic University

This content was sourced from clinicaltrials.gov