Status:

COMPLETED

Female Sexual Dysfunction Intervention

Lead Sponsor:

M.D. Anderson Cancer Center

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Sexual Dysfunction

Eligibility:

FEMALE

18+ years

Brief Summary

The goal of this psychosocial research study is to learn whether a website program called "Tendrils: Sexual Renewal for Women after Cancer " may help female cancer survivors improve their sex lives wh...

Detailed Description

The Tendrils website is designed to give women information about sexual problems related to cancer and its treatment, and the website suggests ways to overcome those problems. The website can be viewe...

Eligibility Criteria

Inclusion

  • Phase I: Woman cancer survivor
  • Phase I: Speaks and reads English well enough to evaluate the website and participate in a focus group
  • Phase II: Had breast cancer or a gynecological cancer diagnosed 1 to 5 years previously
  • Phase II: Has a sexual partner in relationship of at least 6 months' duration.
  • Phase II: Has a score on the Female Sexual Function Inventory below the cut-off criterion indicating sexual dysfunction (i.e. less than 26.55 total score).
  • Phase II: Lives in commuting distance of MDACC so that can attend 3 counseling sessions if randomized to professional treatment group.
  • Phase II: Currently no evidence of active cancer.
  • Phase II: Not receiving any cancer treatment other than hormonal therapy.

Exclusion

  • Phase I: Under age 18
  • Phase II: Under age 18
  • Phase II: Currently in mental health care for a sexual problem.
  • Phase II: BSI-18 at study entry indicates high distress and a visit with project staff confirms that the participant is too distressed to benefit safely from the intervention.
  • Phase II: Cannot arrange for participant to have privacy when accessing internet at home, even if we offer loaner laptop and subsidized internet service.

Key Trial Info

Start Date :

October 1 2007

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

August 1 2013

Estimated Enrollment :

91 Patients enrolled

Trial Details

Trial ID

NCT00614276

Start Date

October 1 2007

End Date

August 1 2013

Last Update

January 9 2015

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

UT MD Anderson Cancer Center

Houston, Texas, United States, 77030

Female Sexual Dysfunction Intervention | DecenTrialz