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WISH, Feasibility of a Factorial Design
NCT07023822 · View on ClinicalTrials.gov ↗
Study Summary
The primary aim of this study is to evaluate the feasibility of testing a multi-component intervention for sexual function using a factorial design.
Conditions Studied
Interventions
- DEVICE Hyaluronic acid (HLA) Vaginal Moisturizer
- DEVICE Polycarbophil Vaginal Moisturizer
- BEHAVIORAL Hypnotic Relaxation
- BEHAVIORAL Progressive Muscle Relaxation (PMR)
Study Locations (1)
Tennessee
- University of Tennessee, College of Nursing — Knoxville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2025-06-16 |
| Est. Completion | 2025-09-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07023822
The ClinicalTrials.gov registry entry for NCT07023822 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Tennessee, Knoxville, which has 34 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Breast Cancer appearing as the primary indexed condition, and to 4 interventions — of which Hyaluronic acid (HLA) Vaginal Moisturizer is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07023822 reports 1 study location spanning 1 distinct geographic area — top geographies include Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT07023822 about?
NCT07023822 is a clinical study titled "WISH, Feasibility of a Factorial Design". The primary aim of this study is to evaluate the feasibility of testing a multi-component intervention for sexual function using a factorial design.
What is the current status of trial NCT07023822?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 18 participants. The study started on 2025-06-16. Estimated completion is 2025-09-30.
What conditions does trial NCT07023822 study?
This clinical trial studies the following conditions: Breast Cancer, Body Image, Vulvovaginal Signs and Symptoms, Sexual Desire Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07023822?
The interventions under investigation include: Hyaluronic acid (HLA) Vaginal Moisturizer (DEVICE), Polycarbophil Vaginal Moisturizer (DEVICE), Hypnotic Relaxation (BEHAVIORAL), Progressive Muscle Relaxation (PMR) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07023822?
This trial is sponsored by The University of Tennessee, Knoxville, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07023822 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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