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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07133087
Enrollment
42
Registered
2025-08-20
Start date
2025-05-06
Completion date
2025-11-15
Last updated
2025-08-20

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

Conditions

Breast Cancer Female

Keywords

breast cancer, body awareness

Brief 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.

Interventions

None listed

Sponsors

Halic University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

for breast cancer survivors: * 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

Exclusion criteria

for breast cancer survivors: * Having a history of rehabilitation due to upper extremity, thoracic, or cervical musculoskeletal disorders within 6 months prior to the breast cancer diagnosis * Having a history of neuromuscular dysfunction * Using medications that may affect neuromuscular performance Inclusion criteria for the control group: * 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

Design outcomes

Primary

MeasureTime frameDescription
Body Awareness ScaleAt the day of enrollmentThe scale consists of 18 items evaluated on a 7-point Likert scale and aims to determine the sensitivity level of body composition through 4 subgroups. The four sub-parameters of the scale are: Changes in Body Processes, Sleep-Wake Cycle, Prediction of Illness Onset, and Prediction of Bodily Reactions.
Disabilities of the Arm, Shoulder and Hand (DASH) QuestionnaireAt the day of enrollmentThe questionnaire will be used to determine individuals' levels of functionality.
Hand Grip Strength AssessmentAt the day of enrollmentA Jamar Hand Dynamometer (Takei Scientific Instruments Co., Ltd - Japan) will be used to measure participants' maximum grip strength
Shoulder Joint Position SenseAt the day of enrollmentShoulder joint position sense will be assessed using the Clinometer smartphone application. Goniometer and inclinometer applications, adapted for both iOS and Android systems, are low-cost methods with proven validity and reliability, accessible to a wide population
European Organisation for Research and Treatment of Cancer QuestionnaireAt the day of enrollmentIt consists of 30 items and includes three subscales for to assess disease spesific quality of life: global health status, functional status, and symptom control.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSeda Saka, PhD
sedasaka@halic.edu.tr05447803417

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026