Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02457780 · ClinicalTrials.gov registry record · NA
Stress Management Program for World Trade Center (WTC) Responders
A NA study, sponsored by Stony Brook University.
- Completed
- Registry status
- NA
- Development phase
- 157
- Enrollment target
NCT02457780: Completed NA study, sponsored by Stony Brook University.
NCT02457780 is a NA study that has completed, run by Stony Brook University. The registered enrollment target is 157 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02457780, a NA study, has completed, sponsored by Stony Brook University.
- COMPLETED
- Registry status
- NA
- Development phase
- 157 participants
- Enrollment target
Study Summary
Many responders to the World Trade Center (WTC) disaster continue to experience significant mental and physical health problems. Two of the most common health problems, post-traumatic stress disorder (PTSD) symptoms and respiratory illness, often occur together. Mental health conditions, such as PTSD, make physical illnesses worse and interfere with treatment. The primary goal of this study is to test a mind-body treatment designed to reduce both PTSD and respiratory symptoms.
Primary Outcome
Assessed via self-report (PTSD Checklist Specific Stressor; PCL-S)
Interventions
- BEHAVIORAL Relaxation Response Resiliency Program (3RP)
- BEHAVIORAL Health Enhancement Program (HEP)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 157 participants |
| Start Date | 2013-08 |
| Est. Completion | 2016-12 |
| Phase | NA |
What the finished NCT02457780 record still lists
NCT02457780 is an interventional study that assigns participants to a tested intervention. The registered 157 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 (89% lower).
The record links to 0 conditions, and to 2 interventions - of which Relaxation Response Resiliency Program (3RP) is the first listed.
NCT02457780 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02457780 about?
NCT02457780 is a clinical study titled "Stress Management Program for World Trade Center (WTC) Responders". Many responders to the World Trade Center (WTC) disaster continue to experience significant mental and physical health problems. Two of the most common health problems, post-traumatic stress disorder (PTSD) symptoms and respiratory illness, often occur together. Mental health conditions, such as PTS...
What is the current status of trial NCT02457780?
This trial is currently completed. It is a NA study. The enrollment target is 157 participants. The study started on 2013-08. Estimated completion is 2016-12.
What interventions are being tested in trial NCT02457780?
The interventions under investigation include: Relaxation Response Resiliency Program (3RP) (BEHAVIORAL), Health Enhancement Program (HEP) (BEHAVIORAL).
Who is sponsoring clinical trial NCT02457780?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02457780's enrollment target sits among peer trials
157 656th of 2000 higher than 1,345 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
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
- NCT05052541 · 157 participants · Phase 3
Safety and Efficacy of Oral Cannabis in Chronic Spine Pain
- NCT05076942 · 157 participants · Phase 2
Groningen International Study on Sentinel Nodes in Vulvar Cancer-III
- NCT06396598 · 157 participants · NA
Electronic Symptom Monitoring Program for Triggered Palliative Referrals in Patients With Thoracic Cancer
- NCT06655246 · 157 participants · Phase 1
A Study of Ziftomenib in Combination With Imatinib in Patients With Advanced Gastrointestinal Stromal Tumors (GIST)
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