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Female Sexual Dysfunction Intervention
This study is currently recruiting participants.
Verified by M.D. Anderson Cancer Center, August 2009
First Received: January 30, 2008   Last Updated: August 14, 2009   History of Changes
Sponsor: M.D. Anderson Cancer Center
Collaborator: National Cancer Institute (NCI)
Information provided by: M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier: NCT00614276
  Purpose

Sexual dysfunction is the most common long-term consequence of cancer treatment, affecting half of survivors of breast and gynecological cancer and many women treated for other cancers. Yet, few women get the help they need for sexual problems.

Our primary objective is to develop and evaluate a multimedia intervention program for women with cancer-related sexual dysfunction.

Tendrils:

A Sexual Renewal Program for Women Surviving Cancer will:

  1. explain the causes of cancer-related sexual dysfunction;
  2. offer self-help strategies to prevent or overcome problems;
  3. advise women on seeking appropriate medical help; and
  4. possibly serve as the core of a counseling program, along with a therapist manual.

Tendrils is aimed at a wide audience, from newly diagnosed to long-term survivors, across cancer sites. Material will be presented with sensitivity to religious and cultural attitudes about sexuality. Animations will illustrate anatomy and physiology. The software will let women use Tendrils in a variety of formats: over the internet, on a CD-Rom, printed out, or as downloaded digital video or audio on a handheld computer or media player. Video vignettes will illustrate problems and strategies. Five female cancer survivors will host the program, sharing their experiences.


Condition Intervention
Sexual Dysfunction
Behavioral: Focus Group
Behavioral: TENDRILS
Behavioral: Questionnaires
Behavioral: Sexual Counseling Sessions

Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: TENDRILS: A Multimedia Intervention for Women's Sexual Dysfunction After Cancer

Resource links provided by NLM:


Further study details as provided by M.D. Anderson Cancer Center:

Primary Outcome Measures:
  • Total score on Female Sexual Function Index (FSFI) [ Time Frame: Baseline, after the 12-week treatment period, and at 3- and 6-month follow-ups. ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 264
Study Start Date: October 2007
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Phase I - Focus Groups Behavioral: Focus Group
To evaluate a multimedia intervention program for women with cancer-related sexual dysfunction.
Behavioral: TENDRILS
Tendrils: A Sexual Renewal Program for Women Surviving Cancer - a website designed to give women information about sexual problems related to cancer and its treatment, and the website suggests ways to overcome those problems.
Behavioral: Questionnaires
The questionnaires ask about your background (such as age, education, relationships), your cancer diagnosis and treatment, and the quality of your life in terms of your health, your general emotions, and your sexual function. The questionnaires take about 30-45 minutes to complete.
Phase II TENDRILS
Phase II - TENDRILS Program only.
Behavioral: TENDRILS
Tendrils: A Sexual Renewal Program for Women Surviving Cancer - a website designed to give women information about sexual problems related to cancer and its treatment, and the website suggests ways to overcome those problems.
Behavioral: Questionnaires
The questionnaires ask about your background (such as age, education, relationships), your cancer diagnosis and treatment, and the quality of your life in terms of your health, your general emotions, and your sexual function. The questionnaires take about 30-45 minutes to complete.
Phase II TENDRILS + Counseling
Phase II - TENDRILS + Sexual Counseling Sessions.
Behavioral: TENDRILS
Tendrils: A Sexual Renewal Program for Women Surviving Cancer - a website designed to give women information about sexual problems related to cancer and its treatment, and the website suggests ways to overcome those problems.
Behavioral: Questionnaires
The questionnaires ask about your background (such as age, education, relationships), your cancer diagnosis and treatment, and the quality of your life in terms of your health, your general emotions, and your sexual function. The questionnaires take about 30-45 minutes to complete.
Behavioral: Sexual Counseling Sessions
Attend 3 sexual counseling sessions at M. D. Anderson.

  Hide Detailed Description

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 viewed on a computer, or parts of it may be printed out or downloaded to portable media players (such as mp3 players). The program includes videos describing women's personal experiences with sexual problems after cancer.

If you are agree to take part in this study, you will have a "screening interview." This interview will help the researchers decide if you are eligible to take part in this study. A member of the research staff will call you on the telephone for this interview, or you may be interviewed in person. You will be asked detailed questions about any sexual problems you may have. You will also be asked about your history of cancer and cancer treatment, and whether you are currently seeing a mental health professional to treat a sexual problem. You must live within what you consider to be commuting distance to M. D. Anderson.

If you are found to be eligible to take part in this study, you will fill out a set of questionnaires over the internet. The questionnaires ask about your background (such as age, education, relationships), your cancer diagnosis and treatment, and the quality of your life in terms of your health, your general emotions, and your sexual function (such as your desire for sex, ability to enjoy sex, and/or any problems with painful sex). In total, the questionnaires will take about 30-45 minutes to complete. You will need to complete at least three-quarters of the questions to continue in the study. If your questionnaires suggest that you are very depressed or upset, a psychologist on the research team will request an in-person interview with you to discuss your feelings. The psychologist will decide whether taking part in the study would be too stressful for you. If this is the case, you will be taken off study. You will also be given a list of referrals for mental health care in the community.

You will be randomly assigned (as in the toss of a coin) to one of 2 groups. There will be an equal chance of being assigned to either group. If you are assigned to Group 1, you will work with the Tendrils program for 12 weeks on your own. If you are assigned to Group 2, in addition to working with the Tendrils program on your own, you will attend 3 sexual counseling sessions at M. D. Anderson.

You will view the Tendrils website over the internet at home over the course of 12 weeks. You will receive your own user name and password to enter the website. If you do not log onto the Tendrils website within 2 weeks after receiving your user name and password, you will be called on the telephone as a reminder. If you do not log on within 4 weeks, you will be taken off study and your password will expire.

To use the Tendrils website, you will read the information, listen to audio interviews of women discussing their sexual problems after cancer (or view videos of the interviews), and practice "homework" that is designed to help to improve your sexual life. The women in the videos discuss, for example, the types of sexual problems they had (such as losing the desire for sex or experiencing pain during sex), how their sexual problems affected their self-esteem or relationships, and what the women did to solve the sexual problems. The videos do not show real people having sexual activity.

The homework may involve hand-writing comments about your sex life. This is just for your own private use, unless you choose to share your writing with your counselor. Writing the comments may take about 15-20 minutes each time. The homework may also involve trying what is called "relaxing touch" with your partner, learning to tense and relax muscles around your vaginal entrance, or trying to change negative thoughts about sex. You will be able to use the website on your own schedule, but it is estimated that you may spend 30-60 minutes per week on the website, plus another 30 minutes per week of homework time. The homework may be practiced alone or with your sexual partner.

When you use the Tendrils website, the system will record how many times you visit the website, how much time you spend on each visit, and which web pages you view. Any time you leave the Tendrils website, the recording stops. The recording only happens on the Tendrils website.

Participants assigned to Group 2 will attend 3 sexual counseling sessions at M. D. Anderson during the 12-week study. Each counseling session will last about an hour. The counselor will be a trained health care professional who will try to help you get the most out of the Tendrils program.

Once a week during the 12 weeks, participants in both Group 1 and Group 2 will be asked to log onto the Tendrils website and answer 3 questions about the website. This is called a diary entry. The questions ask how much time you spent reading printouts from the website, listening to audio or viewing video portions of the website on a portable media player, or doing homework recommended on the website. You will also be asked to answer 1 "knowledge" question each week about what you have learned from using the website.

You will be able to access the website after the 12 weeks, as long as the research study is in progress. However, your password will become inactive if you decide to stop participating in the study before the 12 week treatment period is over, or do not complete questionnaires at the end of 12 weeks.

At the end of the 12 weeks, and then 3 months and 6 months later, you will be asked to complete the same questionnaires that you completed at the beginning of the study. You will not need to answer the medical questions or questions about your background. If the sexual relationship ends during the course of the study, you will still be asked to complete these follow-up questionnaires.

You may be eligible to receive a loaner laptop. If you receive a loaner laptop, you will be asked to return it at the end of the 12 weeks. However, you will still be able to access the website using any computer that has an internet connection, for example at the home of a friend or at a public library. You will also have the option of coming to M. D. Anderson to complete follow-up questionnaires online.

The Tendrils website is hosted on M. D. Anderson's server, which means that the information you give online is protected by a special firewall. Your user name and password will be different than your real name. No identifying information, such as your real name or address, will be entered in the Tendrils website. Only the study chair and 1 or 2 members of the research team will be able to see the list that links your user name and password to your real name. The list of passwords and names will be destroyed at the end of the project.

After returning the last questionnaire at the 6-month follow-up time, your participation in the research study will be finished.

This is an investigational study. Up to 240 women will take part in this study. All will be enrolled at M. D. Anderson.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Women, over 18 years old, with cancer-related sexual dysfunction.

Criteria

Inclusion Criteria:

  1. Phase I: Woman cancer survivor
  2. Phase I: Speaks and reads English well enough to evaluate the website and participate in a focus group
  3. Phase II: Had breast cancer or a gynecological cancer diagnosed 1 to 5 years previously
  4. Phase II: Has a sexual partner in relationship of at least 6 months' duration.
  5. 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).
  6. Phase II: Lives in commuting distance of MDACC so that can attend 3 counseling sessions if randomized to professional treatment group.
  7. Phase II: Currently no evidence of active cancer.
  8. Phase II: Not receiving any cancer treatment other than hormonal therapy.

Exclusion Criteria:

  1. Phase I: Under age 18
  2. Phase II: Under age 18
  3. Phase II: Currently in mental health care for a sexual problem.
  4. 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.
  5. Phase II: Cannot arrange for participant to have privacy when accessing internet at home, even if we offer loaner laptop and subsidized internet service.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00614276

Contacts
Contact: Leslie R Schover, PhD 713-745-2681

Locations
United States, Texas
U.T. M.D. Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030
Principal Investigator: Leslie R Schover, PhD            
Sponsors and Collaborators
M.D. Anderson Cancer Center
Investigators
Principal Investigator: Leslie R Schover, PhD U.T. M.D. Anderson Cancer Center
  More Information

Additional Information:
No publications provided

Responsible Party: U.T. M.D. Anderson Cancer Center ( Leslie Schover, PhD/Professor )
Study ID Numbers: 2006-0340
Study First Received: January 30, 2008
Last Updated: August 14, 2009
ClinicalTrials.gov Identifier: NCT00614276     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by M.D. Anderson Cancer Center:
Sexual Dysfunction
Cancer-related Sexual Dysfunction
Female Cancer Survivors
Tendrils
Website program
Self-help tool
Sexual counseling
Questionnaires

ClinicalTrials.gov processed this record on November 27, 2009