# Enhanced Consent for Symptom Provocation Research

> **NCT01809899** · NA · TERMINATED · sponsor: **Georgetown University** · enrollment: 12 (actual)

## Conditions studied

- Trauma

## Interventions

- **BEHAVIORAL:** Enhanced consent procedure
- **BEHAVIORAL:** Consent as Usual

## Key facts

- **NCT ID:** NCT01809899
- **Lead sponsor:** Georgetown University
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2009-04
- **Primary completion:** 2010-06
- **Final completion:** 2014-08
- **Target enrollment:** 12 (ACTUAL)
- **Why stopped:** Time and funding ran out prior to full recruitment
- **Last updated:** 2018-01-24


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01809899

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01809899, "Enhanced Consent for Symptom Provocation Research". Retrieved via AI Analytics 2026-06-14 from https://api.ai-analytics.org/clinical/NCT01809899. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
