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Spots Global Cancer Trial Database for Effects of Aerobic Cycling Training in Patients With Gynecologic Cancer-related Lower Extremity Lymphedema

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Trial Identification

Brief Title: Effects of Aerobic Cycling Training in Patients With Gynecologic Cancer-related Lower Extremity Lymphedema

Official Title: Effects of Aerobic Cycling Training in Patients With Gynecologic Cancer-related Lower Extremity Lymphedema: A Randomized Comparative Study

Study ID: NCT06200948

Study Description

Brief Summary: Comparison of complete decongestive treatment and complete decongestive treatment + cycling ergometry treatment in patients with gynecologic cancer-related lower extremity lymphedema in terms of quality of life, lower extremity functionality and lower extremity volume measurement

Detailed Description: After being informed about study and potential risks, all patients giving written informed consent will undergo screening period determine eligibility for study entry. The patients who met the eligibility recruitments will get into the assessment. The study will include 63 participants (31 controls and 32 interventions). Simple randomization will be preferred in this study. The coin toss method will be used for simple randomization. Researcher will record demographic and clinical data of the patients and will evaluate the patients' pre-treatment volumes by circumference measurement method. Researcher will evaluate quality of life by lymphedema quality of life questionnaire (LYMQOL) and lower extremity functionality by lower extremity functional scale (LEFS). While the patients in non-cycling group will get only complete decongestive treatment (CDT) for 3 weeks, the patients in cycling group will get CDT+cycling ergometry treatment for 3 weeks.Cycling ergometry treatment will be performed with Voit AT-200 Black Collection horizontal bike for 20 minutes. Exercise intensity will be adjusted to %40-59 of heart rate reserve (HRR). At the end of treatment; Researcher will evaluate volume, functionality and quality of life of the patients again and will compare the two groups in terms of volume measurement, functionality and quality of life.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Ankara Bilkent City Hospital Physical Therapy and Rehabilitation Hospital, Ankara, Bilkent/Çankaya, Turkey

Contact Details

Name: Onur Kara, M.D.

Affiliation: Health Sciences University, Ankara Bilkent City Hospital

Role: PRINCIPAL_INVESTIGATOR

Name: Gül Mete Civelek, M.D.

Affiliation: Health Sciences University, Ankara Bilkent City Hospital

Role: STUDY_DIRECTOR

Name: Meltem Dalyan, M.D.

Affiliation: Health Sciences University, Ankara Bilkent City Hospital

Role: STUDY_CHAIR

Name: Cansu Şahbaz Pirinççi, Pt. (PhD.)

Affiliation: Health Sciences University, Gulhane Physiotherapy and Rehabilitation Faculty

Role: STUDY_CHAIR

Name: Rabia Tarlabölen, Pt.

Affiliation: Health Sciences University, Ankara Bilkent City Hospital

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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