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NCT05700279 · ClinicalTrials.gov registry record · NA
Preventing the Development of Chronic Pain: Treating PTSD at Acute Pain Onset
A NA study of Chronic Pain and PTSD, sponsored by Rush University Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 345
- Enrollment target
- 1
- Study location
NCT05700279 is a NA study of Chronic Pain and PTSD that is actively recruiting participants, run by Rush University Medical Center. The registered enrollment target is 345 participants, below the 771-participant average among 301 other Chronic Pain trials with a reported enrollment target (55% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05700279, a NA study of Chronic Pain and PTSD, is actively recruiting participants, sponsored by Rush University Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 345 participants
- Enrollment target
- 1
- Study location
Study Summary
Although most people recover from acute pain (such as pain caused by injury, surgery, repetitive motion, or unknown causes), many people do not fully recover and will experience chronic pain. Untreated posttraumatic stress disorder (PTSD) appears to be a key risk factor for the transition from acute pain to chronic pain. However, few published studies have addressed the issue of preventing the transition from acute to chronic pain via PTSD reduction. This project will aim to test whether trauma-related PTSD symptoms can be reduced using either Stellate Ganglion Block (SGB) treatment or Cognitive Processing Therapy (CPT), and whether reducing PTSD symptoms can prevent the transition from non-injury based acute pain to chronic pain.
Conditions Studied
Interventions
- BEHAVIORAL Cognitive Processing Therapy
- PROCEDURE Stellate Ganglion Block
Study Locations (1)
Illinois
- Rush University Medical Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 345 participants |
| Start Date | 2023-09-01 |
| Est. Completion | 2027-02-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05700279
The ClinicalTrials.gov registry entry for NCT05700279 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 345 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 771-participant average among 301 other Chronic Pain trials with a reported enrollment target (55% lower). The listed sponsor is Rush University Medical Center, which has 320 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Chronic Pain appearing as the primary indexed condition, and to 2 interventions - of which Cognitive Processing Therapy is the first listed.
NCT05700279 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT05700279 about?
NCT05700279 is a clinical study titled "Preventing the Development of Chronic Pain: Treating PTSD at Acute Pain Onset". Although most people recover from acute pain (such as pain caused by injury, surgery, repetitive motion, or unknown causes), many people do not fully recover and will experience chronic pain. Untreated posttraumatic stress disorder (PTSD) appears to be a key risk factor for the transition from acute...
What is the current status of trial NCT05700279?
This trial is currently recruiting. It is a NA study. The enrollment target is 345 participants. The study started on 2023-09-01. Estimated completion is 2027-02-01.
What conditions does trial NCT05700279 study?
This clinical trial studies the following conditions: Chronic Pain, PTSD.
What interventions are being tested in trial NCT05700279?
The interventions under investigation include: Cognitive Processing Therapy (BEHAVIORAL), Stellate Ganglion Block (PROCEDURE).
Who is sponsoring clinical trial NCT05700279?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05700279 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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