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NCT06253182 · ClinicalTrials.gov registry record · NA
Psychosexual Educational Partners Program (PEPP)
A NA study of Breast Cancer and Gynecologic Cancer, sponsored by The University of Tennessee, Knoxville.
- Active
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT06253182 is a NA study of Breast Cancer and Gynecologic Cancer that is active but no longer recruiting, run by The University of Tennessee, Knoxville. The registered enrollment target is 60 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06253182, a NA study of Breast Cancer and Gynecologic Cancer, is active but no longer recruiting, sponsored by The University of Tennessee, Knoxville.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare two Psychosexual Educational programs for women who have completed treatment for breast or gynecological cancer and their partners in preparation for a well-powered phase III study. The investigators plan to enroll 30 dyads in a 2-arm pilot randomized controlled trial (RCT). The primary aim will be to assess the preliminary efficacy of the Psychosexual Educational Partners Program (PEPP) on sexual communication.
Conditions Studied
Interventions
- BEHAVIORAL Self-Guided PEPP Intervention Workbook
- BEHAVIORAL Self-Guided PEPP Education Workbook
Study Locations (1)
Tennessee
- University of Tennessee Knoxville - Knoxville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-04-02 |
| Est. Completion | 2025-09-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06253182
The ClinicalTrials.gov registry entry for NCT06253182 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The listed sponsor is The University of Tennessee, Knoxville, which has 81 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which Self-Guided PEPP Intervention Workbook is the first listed.
NCT06253182 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT06253182 about?
NCT06253182 is a clinical study titled "Psychosexual Educational Partners Program (PEPP)". The purpose of this study is to compare two Psychosexual Educational programs for women who have completed treatment for breast or gynecological cancer and their partners in preparation for a well-powered phase III study. The investigators plan to enroll 30 dyads in a 2-arm pilot randomized controll...
What is the current status of trial NCT06253182?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-04-02. Estimated completion is 2025-09-30.
What conditions does trial NCT06253182 study?
This clinical trial studies the following conditions: Breast Cancer, Gynecologic Cancer, Sexual Dysfunction, Partner Communication.
What interventions are being tested in trial NCT06253182?
The interventions under investigation include: Self-Guided PEPP Intervention Workbook (BEHAVIORAL), Self-Guided PEPP Education Workbook (BEHAVIORAL).
Who is sponsoring clinical trial NCT06253182?
This trial is sponsored by The University of Tennessee, Knoxville, which has 81 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06253182 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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