Last reviewed · How we verify
NCT03504722: RESCUE
Evaluating the Feasibility of RESCUE: An Adjunctive HAI-Based Intervention for Veterans With PTSD
NA trial testing RESCUE in PTSD in 57 participants. Completed in 1 September 2019.
31 August 2019
Quick facts
| Lead sponsor | Charleston Research Institute |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 57 |
| Start date | 27 September 2016 |
| Primary completion | 31 August 2019 |
| Estimated completion | 1 September 2019 |
| Sites | 1 location across United States |
Drugs / interventions tested
- RESCUE — full drug profile →
- Prolonged Exposure
Conditions studied
- PTSD — all drugs for PTSD →
Sponsor
Charleston Research Institute
Who can join
Adults 18 to 65, any sex, with PTSD. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To develop and pilot test feasibility, acceptability, and efficacy of an adjunct intervention for use with Empirically Based Treatments (EBT) for posttraumatic stress disorder (PTSD) in order to increase treatment engagement, treatment completion, and improve treatment response regarding emotional numbing symptoms. Recovery through Engagement with Shelter Canines, Understanding, and Exposure (RESCUE), is an adjunctive, Human Animal Interaction (HAI) intervention that will be developed for integration into Prolonged Exposure (PE) treatment. Feasibility, acceptability, and initial efficacy testing of the experimental treatment condition will be conducted in a pilot crossover randomized controlled trial (RCT) conducted with 75 veterans with PTSD randomly assigned to RESCUE delivered with PE (RESCUE+PE) or to standard PE initiation (PE + delayed RESCUE).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
An adjunctive human-animal interaction intervention for veterans with PTSD: study protocol for a randomized controlled trial.
Grubaugh AL, Myers US, Keller SM, Wangelin BC, et al · · 2019 · cited 2× · PMID 31881993 · DOI 10.1186/s13063-019-3877-3
Verify or expand the search:
- PubMed search for NCT03504722
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of RESCUE
Trials testing the same drug.
- NCT06779617 — UMMS Sepsis Early Prediction Score (SEPSys) and RESCUE Score Combined Clinical Trial · NA · not yet recruiting
Other recruiting trials for PTSD
Currently open trials in the same condition.
- NCT07473505 — Integrative Bilateral Cervical Sympathetic Blocks for Trauma-Related Symptoms in Special Operations Veterans: A Prospect · recruiting
- NCT07010757 — Testing an Integrated PTSD and Weight Management Intervention: A Hybrid Type 1 Trial · NA · recruiting
- NCT07372586 — Behavioral Health Collaborative Care Model in an ICU Recovery Clinic · NA · recruiting
- NCT07390786 — Behavioral Health Collaborative Care Model in Post-ICU Clinic Family Pilot · NA · recruiting
- NCT07469098 — Group vs Individual MDMA-Assisted Therapy for PTSD After the October 7, 2023 Events · Phase 2 · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03504722 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Charleston Research Institute
- Last refreshed: 22 January 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03504722.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing