Exploring a new intervention for somatic flashbacks in PTSD
An Intervention for Somatic Flashbacks in Post-Traumatic Stress Disorder: a Feasibility Study
NA · University College, London · NCT05996913
This study is trying out a new way to help adults with PTSD manage somatic flashbacks by using a technique called Imagery Rescripting to see if it makes them feel better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 15 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | University College, London (other) |
| Locations | 2 sites (London and 1 other locations) |
| Trial ID | NCT05996913 on ClinicalTrials.gov |
What this trial studies
This trial investigates the feasibility and acceptability of an intervention aimed at managing somatic flashbacks in adults with Post-Traumatic Stress Disorder (PTSD). The intervention centers around Imagery Rescripting (ImRs), which is designed to help participants process and cope with their traumatic memories. The study will assess how well this intervention is received and whether it leads to improvements in the frequency and intensity of somatic flashbacks and overall PTSD symptoms. By focusing on the often-overlooked phenomenon of somatic flashbacks, this research aims to fill a gap in current PTSD treatment approaches.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and above who have a DSM-5 diagnosis of PTSD or Complex PTSD and are currently experiencing somatic flashbacks.
Not a fit: Patients currently receiving another trauma-focused intervention or those with active suicidal intent may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could provide a novel therapeutic option for patients suffering from somatic flashbacks associated with PTSD.
How similar studies have performed: While there is limited empirical research on managing somatic flashbacks, the approach of using trauma-focused therapies has shown success in treating PTSD more broadly.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria * Aged 18 and above * DSM-5 diagnosis of PTSD or Complex PTSD * Participants who are currently experiencing somatic flashbacks * Willing and able to provide written informed consent to treatment Exclusion criteria: * Currently receiving another trauma-focussed intervention * Active suicidal intent or recent (past 8 weeks) suicide attempt * Currently abusing substances * Participants whose participation in the study is not considered in their best interest by the clinical team at Traumatic Stress Clinic and Woodfield Trauma Service * Participants who do not consent to the intervention sessions being recorded * Participants who do not consent to their assessment information being made available to the trainee clinical psychologist carrying out the intervention
Where this trial is running
London and 1 other locations
- Traumatic Stress clinic — London, United Kingdom (RECRUITING)
- Woodfield Trauma service — London, United Kingdom (RECRUITING)
Study contacts
- Principal investigator: Livia Ottisova, Doctorate — Camden and Islington NHS
- Study coordinator: JOE CAMPBELL
- Email: joe.campbell.21@ucl.ac.uk
- Phone: 07772253838
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Post-traumatic Stress Disorder