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The Validity and Reliability of FIT-HaNSA in Breast Cancer Patients

G

Gazi University

Status

Unknown

Conditions

Breast Cancer
Upper Extremity Dysfunction
FIT-HaNSA

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Breast cancer is the most common type of cancer among women and covers 25% of all cancers. After mastectomy and reconstruction, many patients develop various upper extremity complications such as joint movement limitation, pain, lymphedema, and axillary cord. Because of such upper extremity problems, evaluation and treatment of upper extremity functions are important. Upper extremity functions are generally evaluated with questionnaires filled out by the patients themselves and which reflect their own perspectives subjectively. However, these questionnaires cannot reflect the observations and evaluations of the clinicians. Performance tests are important for clinicians to make decisions.

With this study, we want to examine the usability of the FIT-HaNSA test in the evaluation of upper extremity functions in patients with breast cancer. Our hypothesis; The FıtHaNSA test is successful in evaluating the upper extremity function in patients with breast cancer.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Those whose treatments for breast cancer have been completed 18 years and over

Exclusion criteria

  • Have a history of upper extremity surgery, excluding breast cancer surgery Have a history of upper extremity trauma Those who have orthopedic, neurological, rheumatological or cognitive impairments that may interfere with the application of the test.

Trial design

30 participants in 2 patient groups

Patients with breast cancer
Description:
Breast cancer patients with or without breast cancer surgery, with or without mastectomy, with or without lymphedema
Control group
Description:
Healty individuals with no disease

Trial contacts and locations

1

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Central trial contact

inci ayas; ilke keser

Data sourced from clinicaltrials.gov

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