Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00097305 · ClinicalTrials.gov registry record · Phase 2
Body-Oriented Therapy for Sexual Abuse Recovery
A Phase 2 study of Post Traumatic Stress Disorder and Dissociation, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- Completed
- Registry status
- Phase 2
- Development phase
- 24
- Enrollment target
- 1
- Study location
NCT00097305: Completed Phase 2 study of Post Traumatic Stress Disorder and Dissociation, sponsored by National Center for Complementary and Integrative Health (NCCIH).
NCT00097305 is a Phase 2 study of Post Traumatic Stress Disorder and Dissociation that has completed, run by National Center for Complementary and Integrative Health (NCCIH). The registered enrollment target is 24 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00097305, a Phase 2 study of Post Traumatic Stress Disorder and Dissociation, has completed, sponsored by National Center for Complementary and Integrative Health (NCCIH).
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 24 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to examine and compare the effects of two body therapy approaches in women who have experienced child sexual abuse.
Conditions Studied
Interventions
- BEHAVIORAL Body-Oriented Therapy
- BEHAVIORAL Standardized Massage Therapy
Study Locations (1)
Washington
- University of Washington School of Nursing - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2002-09 |
| Phase | Phase 2 |
What the finished NCT00097305 record still lists
NCT00097305 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (96% lower).
The record links to 3 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Body-Oriented Therapy is the first listed.
NCT00097305 reports a single indexed study location in Washington.
Frequently Asked Questions
What is clinical trial NCT00097305 about?
NCT00097305 is a clinical study titled "Body-Oriented Therapy for Sexual Abuse Recovery". The purpose of this study is to examine and compare the effects of two body therapy approaches in women who have experienced child sexual abuse.
What is the current status of trial NCT00097305?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2002-09.
What conditions does trial NCT00097305 study?
This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Dissociation, Child Abuse, Sexual.
What interventions are being tested in trial NCT00097305?
The interventions under investigation include: Body-Oriented Therapy (BEHAVIORAL), Standardized Massage Therapy (BEHAVIORAL).
Who is sponsoring clinical trial NCT00097305?
This trial is sponsored by National Center for Complementary and Integrative Health (NCCIH), which has 203 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00097305 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Post Traumatic Stress Disorder
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00097305's enrollment target sits among peer trials
24 225th of 262 higher than 37 of 262 other Post Traumatic Stress Disorder trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder 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
-
Department of Defense PTSD Adaptive Platform Trial - Intervention A - Fluoxetine
RECRUITING · Phase 2
-
Facilitation of Extinction Retention and Reconsolidation Blockade by IV Allopregnanolone in PTSD.
RECRUITING · Phase 2
-
Facilitation of Extinction Retention and Reconsolidation Blockade in PTSD
RECRUITING · Phase 2
-
Department of Defense PTSD Adaptive Platform Trial - Master Protocol
RECRUITING · Phase 2
-
MDMA for AUD/PTSD Comorbidity
RECRUITING · Phase 2
-
Enhancing Transdiagnostic Mechanisms of Cognitive Dyscontrol (R33)
RECRUITING · Phase 2
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02331979 · 24 participants · NA
Improving Bladder Function in SCI by Neuromodulation
- NCT03096197 · 24 participants · NA
Exoskeleton and Spinal Cord Stimulation for SCI
- NCT03223922 · 24 participants · NA
Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases
- NCT03326921 · 24 participants · Phase 1
HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia