Clinical Trials Directory

Trials / Unknown

UnknownNCT05625126

Evaluation of a Rumination Intervention for Individuals With PTSD: A Case Series

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
16 (actual)
Sponsor
University of Oxford · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

After a traumatic event, it is common for thoughts to run through our minds over and over again. Typically, these include unanswerable questions like "why did this happen to me?", "what if I had done something differently?" Dwelling or ruminating on the past like this is often unhelpful and research has shown that it increases our chances of developing posttraumatic stress disorder (PTSD), a debilitating stress reaction. Once PTSD is in place, research shows that ruminating keeps the disorder going. It is unknown to what extent targeting rumination with an intervention to reduce its recurrence may help to alleviate PTSD symptoms. While rumination interventions using evidence-based cognitive behavioural therapy (CBT) have shown highly promising results in depression and anxiety research, no previous study has evaluated a stand-alone rumination intervention for individuals with PTSD. The aim of this study is to examine the impact of a one-session online Rumination Intervention designed to reduce rumination in a small sample of 14 individuals who are currently awaiting treatment for PTSD in a British national mental health (NHS) service. The study will explore whether the Rumination Intervention reduces PTSD-related rumination, as well as PTSD and depression symptoms. It will also investigate how feasible and acceptable the intervention is for participants. If the findings are promising, the intervention could be tested in a larger clinical study in the future. Results may help inform online interventions for PTSD.

Detailed description

Please note: This study adopts a within and between-subjects concurrent multiple baseline A-B design will be used for this study. Due to the format of a case series, there will be no control group and no blinding. Participants will be compared to their own baseline (within) and between groups (delayed baseline for arm 2), meaning that individuals with a 3-week baseline will be compared to individuals with a 5-week baseline. This will be an experimental framework.

Conditions

Interventions

TypeNameDescription
OTHERRumination Intervention for individuals with PTSDThe intervention utilises evidence-based cognitive behavioural therapy (CBT) techniques.

Timeline

Start date
2022-12-07
Primary completion
2023-03-31
Completion
2023-06-30
First posted
2022-11-22
Last updated
2023-04-04

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT05625126. Inclusion in this directory is not an endorsement.