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Not yet recruiting Not applicable NCT07548476

Acupuncture and Exercise for EV-Pembro-Induced Peripheral Neuropathy

No applicable phase (e.g. observational)
Conditions: Metastatic Bladder Cancer Peripheral Neuropathy Advanced Urothelial Cancer Metastatic Urothelial Cancer

Sponsor: Dana-Farber Cancer Institute

trial.available_in: БГ
Overview
The goal of this study is to evaluate the feasibility and preliminary efficacy of a combined acupuncture and exercise intervention for the management of chemotherapy-induced peripheral neuropathy (CIPN) in participants with metastatic bladder cancer receiving enfortumab vedotin (EV) and pembrolizumab (Pembro). The names of the two study groups in this research study are: * Acupuncture + Virtual Exercise (AVE) * Virtual Exercise Only (VE)
Description
The goal of this study is to evaluate the feasibility and preliminary efficacy of a combined acupuncture and exercise intervention for the management of chemotherapy-induced peripheral neuropathy (CIPN) in participants with metastatic bladder cancer receiving enfortumab vedotin (EV) and pembrolizumab (Pembro). CIPN is a side effect of some kinds of chemotherapy, and can lead to pain, numbness, tingling, swelling, or muscle weakness, primarily in the hands and feet and may persist for months or even years after chemotherapy ends. Acupuncture involves using tiny needles to stimulate nerves and pathways in the body, and early research shows it might be helpful in reducing symptoms of CIPN. Participants will be randomized in a 1:1 fashion into one of two study groups: AVE Arm: Acupuncture + Virtual Exercise or VE Arm: Virtual Exercise Only. Randomization means a participant is placed into a study group by chance. The research study procedures include screening for eligibility, questionnaires, sensory tests, cycling test, and physical performance tests. Participation in this research study is expected to last about 12 weeks. About 50 people will take part in this study.
Who can participate
Inclusion Criteria: * Age ≥ 18 years old * Diagnosed with pathologically proven advanced or metastatic urothelial cancer (mUC) * Planning to receive treatment with EV-Pembro or have received up to two cycles of EV-Pembro treatment with enrollment occurring prior to the start of the third cycle * Self-reported ability to walk for 6 minutes and/or 2 blocks * Deemed acceptable for exercise by their treating provider * Sedentary, currently engaging in less than or equal to 60 minutes of moderate or vigorous structured exercise/week, as assessed by the Godin Leisure-Time Exercise Questionnaire * Willing to adhere to all study-related procedures, including randomization to one of the two possible acupuncture treatments * Eligible per verbally administered Physical Activity Readiness Questionnaire (PAR-Q+) * Referrals to physical therapy are allowed during the study if necessary; and * Participants taking any of medications listed below must be on a stable regimen, with no changes in the past three months. Use of these medications may continue while on study. * Duloxetine, amitriptyline, nortriptyline, gabapentin, and pregabalin Exclusion Criteria: * History of peripheral neuropathy prior to EV-Pembro initiation * Patients with a pacemaker or other electronically charged medical device; or * Participate in more than 60 minutes of moderate or vigorous structured exercise/week We will not include the following special populations: * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers \< 18 years) * Pregnant women * Prisoners
Interventions
Acupuncture
PROCEDURE
Exercise
BEHAVIORAL
Locations 1
United States (1)
Dana Farber Cancer Institute
Boston , Massachusetts
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
02.10.2026
Completion date
02.03.2027
Registry ID
NCT07548476
Source
clinicaltrials.gov
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