Pre-Rehabilitation for Female Patients Undergoing Pelvic Radiotherapy

Recruiting N/A Interventional Study
Dyspareunia Pelvic Pain Sexual Dysfunction Radiation Toxicity
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
20 (estimated)
Sponsor
Indiana University · Other
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About This Trial
The purpose of this study is to examine the feasibility of adding pre-rehabilitation pelvic health physical therapy to standard of care radiation therapy treatment plan for female patients who have been diagnosed with cervical, vaginal, vulvar, uterine, or anal cancer and are a candidate for curative pelvic radiation with external beam. Participants will receive education on using a vaginal dilato…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Female 2. ≥ 18 years old at the time of informed consent 3. Ability to provide written informed consent and HIPAA authorization 4. Primary diagnosis of cervical, vaginal, vulvar, uterine, or anal cancer 5. Candidate for curative pelvic radiation with external beam, with or wi…
Contacts

Namita Agrawal, MD

(317)944-2524

agrawaln@indiana.edu

CONTACT

Sarah Dutkevich, RN

(317)278-5618

sdutkevi@iu.edu

CONTACT