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NCT04713501 · ClinicalTrials.gov registry record · NA

Program for Alleviating and Resolving Trauma and Stress 1

A NA study, sponsored by Cambridge Health Alliance.

Completed
Registry status
NA
Development phase
15
Enrollment target

NCT04713501: Completed NA study, sponsored by Cambridge Health Alliance.

NCT04713501 is a NA study that has completed, run by Cambridge Health Alliance. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04713501, a NA study, has completed, sponsored by Cambridge Health Alliance.

COMPLETED
Registry status
NA
Development phase
15 participants
Enrollment target

Study Summary

This single-arm pilot study (Phase 1) will test the preliminary efficacy of a virtually delivered, live-online 16-week group model of Internal Family Systems (IFS) for individuals with PTSD, called the PARTS program, on PTSD symptoms measured by Clinician-Administered PTSD Scale (CAPS-5). In addition, feasibility, acceptability, and effects on self-report PTSD and disturbances of self-organization (DSO) will be secondary outcomes.

Primary Outcome

The primary aim of this study is to examine the preliminary efficacy of a live-online version of the PARTS program on PTSD symptoms measured by reduction in CAPS-5 over 24 weeks. The CAPS-5 is a 30-item questionnaire administered by a trained interviewer and is considered the "gold standard" assessment for PTSD diagnosis and symptoms as defined by the DSM-5. This measure also assesses the duration of symptoms, impact of symptoms on aspects of the participant's life, and if the participant meets

Interventions

  • BEHAVIORAL PARTS Program

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2020-12-22
Est. Completion 2021-07-31
Phase NA
Cambridge Health Alliance

45 total trials

What the finished NCT04713501 record still lists

NCT04713501 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which PARTS Program is the first listed.

NCT04713501 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04713501 about?

NCT04713501 is a clinical study titled "Program for Alleviating and Resolving Trauma and Stress 1". This single-arm pilot study (Phase 1) will test the preliminary efficacy of a virtually delivered, live-online 16-week group model of Internal Family Systems (IFS) for individuals with PTSD, called the PARTS program, on PTSD symptoms measured by Clinician-Administered PTSD Scale (CAPS-5). In additio...

What is the current status of trial NCT04713501?

This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2020-12-22. Estimated completion is 2021-07-31.

What interventions are being tested in trial NCT04713501?

The interventions under investigation include: PARTS Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT04713501?

This trial is sponsored by Cambridge Health Alliance, which has 45 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04713501's enrollment target sits among peer trials

15 1881st of 2000 higher than 92 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

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Source: ClinicalTrials.gov NCT04713501, the US trial registry maintained by the National Library of Medicine. NCT04713501 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.