Cervical or Endometrial Cancer and Sexual Health Study
NCT00134316 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31
Last updated 2011-03-02
Summary
Aim #1. To investigate the efficacy of the psychoeducational intervention (PED) on sexual arousal.
H1: Compared to a control group and to baseline, PED will result in significant improvement in:
* self-reported subjective sexual arousal;
* self-reported genital sensitivity;
* psychophysiological sexual arousal.
Aim #2. To investigate the efficacy of the PED on self-reported orgasm, sexual desire, distress, and relationship satisfaction.
H2: Compared to a control group and to baseline, PED will result in significant improvement in self-reported orgasmic experience, sexual desire, sexual distress, and relationship satisfaction.
Aim #3. To investigate the efficacy of the PED on depressive symptoms and quality of life.
H3: Compared to a control group and to baseline, PED will result in significant improvement in self-reported depressive symptoms and quality of life.
Conditions
- Sexual Dysfunctions, Psychological
Interventions
- BEHAVIORAL
-
psychoeducational intervention
three 75 minute long individual psychoeducational sessions
Sponsors & Collaborators
-
Canadian Institutes of Health Research (CIHR)
collaborator OTHER_GOV -
University of British Columbia
lead OTHER
Principal Investigators
-
Rosemary Basson, FCRP (UK) · University of British Columbia
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 19 Years
- Max Age
- 65 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-08-31
- Primary Completion
- 2009-11-30
- Completion
- 2010-06-30
Countries
- Canada
Study Locations
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