Gynecologic Cancer Lymphedema Questionnaire as a Clinical Care Tool to Identify Lower Extremity Lymphedema

Memorial Sloan Kettering Cancer Center (MSK)

Status: Completed

Conditions: Uterine Cancer; Vaginal Cancer; Lymphedema; Ovarian Cancer

Treatments: Behavioral: GCLQ lymphedema symptom assessment questionnaire; Behavioral: limb volume measurements and GCLQ lymphedema symptom assessment questionnaire

Study type: Observational

Funder types: Other

Identifiers

NCT00944944

09-077

Details and patient eligibility

About

The purpose of this study is to evaluate if the Gynecologic Cancer Lymphedema Questionnaire (GCLQ) truly detects symptoms or signs of lower extremity lymphedema in patients with diagnosed lower extremity lymphedema. Lymphedema is a chronic condition in which fluid accumulates in the tissues of the body. Many cancer survivors are living with discomfort and changes in their activities due to limb swelling following cancer treatment. If the GCLQ is able to do detect signs and symptoms of lymphedema, the investigators hope to use it as a tool in the clinical care setting to help identify women at risk for or with lymphedema. In the future, this could improve clinical care through the use of a more simple and feasible way to identify lower extremity lymphedema than measuring limbs.

Enrollment: 58 patients

Sex: Female

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Study group of Gynecologic cancer survivors with Lymphedema
• Documented lower extremity lymphedema
• History of a primary diagnosis of gynecologic cancer (vulvar, cervical and uterine only)
• History of surgery for gynecologic cancer including lymph node removal
• No evidence of disease or active treatment
• At least 21 years of age
• Able and willing to provide informed consent
• English fluency Comparison Group of Gynecologic Cancer Survivors without Lymphedema
• No history of lower extremity lymphedema or presence of lymphedema confirmed by limb volume measurements at the time of study participation
• History of a primary diagnosis of gynecologic cancer (vulvar, cervical and uterine only)
• History of surgery for gynecologic cancer including lymph node removal
• No evidence of disease or active treatment
• At least 21 years of age
• Able and willing to provide informed consent
• English fluency

Exclusion criteria

• Inability to participate in an informed consent process
• Patients with a psychiatric disorder precluding response to the survey

Trial design

58 participants in 2 patient groups

Gyn Pts with lymphedema

Treatment:

Behavioral: GCLQ lymphedema symptom assessment questionnaire

Gyn Pts without Lymphedema

Treatment:

Behavioral: limb volume measurements and GCLQ lymphedema symptom assessment questionnaire