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Nonattachment Training for Post Traumatic Stress Recovery

NCT06683027 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2024-11-12

No results posted yet for this study

Summary

This pilot study aims to investigate the effectiveness of a novel, co-created intervention based on principles of nonattachment for individuals recovering from Post-Traumatic Stress (PTS).

Objectives include:

1. Determine whether participants undertaking nonattachment-based training have higher levels of nonattachment (as indicated by NAS Scale) after completing program.
2. Determine whether nonattachment levels are impacted after 3 months
3. Determine whether PTS symptoms are impacted by training/intervention

Conditions

  • Post Traumatic Stress Symptoms
  • PTSD

Interventions

BEHAVIORAL

Nonattachment for Post Traumatic Stress

This study seeks to cultivate nonattachment specifically for the alleviation of symptoms of post-traumatic stress. This is an 8-week online intervention where, following a Qualrics-hosted pre-screen, users are directed to www.npts.online to use as they wish. Users are then solicited to re-take quantitative assessments, and a subset of 10 (target number) will be recruited for a qualitative interview regarding their experience of the intervention. A final prompt for assessment re-takes will follow at 3 months post-intervention to determine longitudinal efficacy.

Sponsors & Collaborators

  • University of Derby

    lead OTHER

Principal Investigators

  • William Van Gordon, PhD · University of Derby

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-18
Primary Completion
2025-01-31
Completion
2025-03-01

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06683027 on ClinicalTrials.gov