Can a brief therapy beat standard PTSD care?
NCT ID NCT07460817
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares a new, shorter therapy for Post-Traumatic Stress Disorder (PTSD) to standard treatments. Researchers want to see if the brief approach works just as well at reducing symptoms. About 82 adults with PTSD will take part. The main goal is to measure changes in PTSD symptoms and quality of life.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 82 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2025
- Expected to finish
-
Dec 2029
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants must have experienced at least one traumatic experience throughout their lifetime * Participants must meet the DSM-5 criteria for PTSD, or subthreshold PTSD * The following DSM-5 criteria must be fulfilled: * A (exposure to traumatic stressor), * in addition to three out of four of the following symptom-clusters; * B (intrusion), * C (avoidance), * D (negative alterations in cognitions and mood), * E (alterations in arousal and reactivity) * A marked decline in functioning and symptom persistence for over a month Exclusion Criteria: * ongoing psychotic disorders, or a history of psychosis, * severe suicidal ideation, * bipolar disorder, * BMI index too low to benefit from psychological interventions, * severe alcohol or substance dependence, * serious somatic illness or brain damage, * participation in concurrent psychotherapy.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Post-traumatic stress disorder are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
University of Bergen
Bergen, Norway
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Five sessions to quiet trauma nightmares in bipolar disorder
- Can training hospital staff in Trauma-Informed care make childbirth safer?
- Scientists probe brain's reward system in mental illness
- Can a mindfulness class help veterans with concussion and PTSD?
- Can MDMA plus therapy help veterans fight both PTSD and alcohol addiction?
- Can talk therapies quiet the trauma of violence?