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NCT06697548 · ClinicalTrials.gov registry record · NA
Conservative Care for Pelvic Pain (C2P2) in Women Service Members
A NA study, sponsored by Baylor University.
- Not yet
- Registry status
- NA
- Development phase
- 300
- Enrollment target
NCT06697548: Clinical Trial NA study, sponsored by Baylor University.
NCT06697548 is a NA study that has not yet begun recruiting, run by Baylor University. The registered enrollment target is 300 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06697548, a NA study, has not yet begun recruiting, sponsored by Baylor University.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 300 participants
- Enrollment target
Study Summary
This study will test the effectiveness of emerging conservative interventions for treatment of chronic pelvic pain (CPP) that can be performed without intravaginal specialization. Participants with CPP will be randomly assigned to one of three groups. The first group will receive treatment based on what they normally would receive, including medications, education, and exercise (Usual Care Group). The second group will receive contemporary non-vaginal treatment including manual therapy, dry needling, and specific breathing training (Emerging Field-expedient Care Group). The third group will receive intravaginal treatment by a pelvic health specialist (Gold-standard Intravaginal Specialist Care Group). Participants will be asked about their pain and symptoms and have measurements taken of their pelvic and back muscles after 1, 3, 6, and 12 months. In addition to seeing which treatments work best, clinical decision tools (using medical and trauma history along with clinical examination) will be developed to identify women with CPP likely to respond favorably to non-vaginal conservative interventions. This study will help determine the best non-vaginal treatment strategies for women with CPP and help clinicians quickly determine which patients are likely to benefit from treatment by non-pelvic health physical therapists (e.g., in theater), vs. patients who should be referred for pelvic health specialty care.
Primary Outcome
The Pelvic Floor Distress Inventory (PFDI-20) is a 20-item questionnaire that assesses the frequency and severity of pelvic floor symptoms. It consists of 3 subscales: the pelvic floor distress inventory 6 (POPDI-6), the colorectal anal distress inventory 8 (CRADI-8), and the urinary distress inventory 6 (UDI-6). Each question is rated on a scale of 0-4 with 0 representing "no symptoms," and 4 representing "quite a bit." Higher scores represent more bothersome symptoms.
Interventions
- OTHER Pain Neuroscience Education
- OTHER Lumbopelvic and Hip Therapeutic Exercise
- OTHER Extrapelvic Manual Therapy
- OTHER Extrapelvic Dry Needling
- OTHER Deep Paced Diaphragmatic Breathing Training
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2025-01 |
| Est. Completion | 2028-06 |
| Phase | NA |
What is known before NCT06697548 opens enrollment
NCT06697548 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (79% lower).
The record links to 0 conditions, and to 5 interventions - of which Pain Neuroscience Education is the first listed.
NCT06697548 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06697548 about?
NCT06697548 is a clinical study titled "Conservative Care for Pelvic Pain (C2P2) in Women Service Members". This study will test the effectiveness of emerging conservative interventions for treatment of chronic pelvic pain (CPP) that can be performed without intravaginal specialization. Participants with CPP will be randomly assigned to one of three groups. The first group will receive treatment based on ...
What is the current status of trial NCT06697548?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 300 participants. The study started on 2025-01. Estimated completion is 2028-06.
What interventions are being tested in trial NCT06697548?
The interventions under investigation include: Pain Neuroscience Education (OTHER), Lumbopelvic and Hip Therapeutic Exercise (OTHER), Extrapelvic Manual Therapy (OTHER), Extrapelvic Dry Needling (OTHER), Deep Paced Diaphragmatic Breathing Training (OTHER).
Who is sponsoring clinical trial NCT06697548?
This trial is sponsored by Baylor University, which has 33 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06697548's enrollment target sits among peer trials
300 330th of 2000 higher than 1,630 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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