Actively Recruiting

Age: 25Years - 75Years
FEMALE
Healthy Volunteers
NCT07133087

Body Awareness, Upper Extremity Function, and Quality of Life in Breast Cancer Survivors

Led by Halic University · Updated on 2025-08-20

42

Participants Needed

2

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Body Awareness, Upper Extremity Function, and Quality of Life in Breast Cancer Survivors

Who Can Participate

Age: 25Years - 75Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Woman aged 25 to 75 years
  • Diagnosed with Stage 0 to III breast cancer
  • Completed primary breast cancer treatments (surgery, chemotherapy, or radiation) within 6 months before assessment
  • Received medical clearance from a physician
  • Underwent breast-conserving surgery or mastectomy due to breast cancer
  • Willing to participate voluntarily
  • Control group women matched by age within 5 years and body mass index within �b13 kg/m�b2 to breast cancer survivor group
  • Control group matched for hand dominance with breast cancer survivor group
Not Eligible

You will not qualify if you...

  • History of rehabilitation for upper extremity, chest, or neck muscle/bone disorders within 6 months before breast cancer diagnosis
  • History of neuromuscular dysfunction
  • Use of medications affecting neuromuscular performance
  • Control group exclusion includes history of neuromuscular dysfunction
  • Control group exclusion includes use of medications affecting neuromuscular performance
  • Control group exclusion includes rehabilitation history for upper extremity, chest, or neck disorders within last 6 months

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Halic University

Istanbul, Turkey (Türkiye)

Actively Recruiting

2

Yeditepe Hospital

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

S

Seda Saka, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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