Clinical trial Recruiting at 1 site Interventional Ages 18 and up

SEE FAR CBT for Adults With PTSD

Official title: A Clinical Study Evaluating the Effects of a SEE FAR CBT Intervention on Psychological Outcomes in Adults With Posttraumatic Stress Disorder.

Run by Community Stress Prevention Center · NCT07720674 · Data updated 2026-11-12

This 12-week, one-on-one SEE FAR CBT program tests a trauma-focused therapy to see if PTSD symptoms improve in adults 18 and older.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorCommunity Stress Prevention Center
Academic / other
Locations1 site (Kiryat Shmona)
StatusRecruiting
StartedJuly 2026
Main results expectedDecember 2027
Study endsMarch 2028
Registry record updatedJuly 22, 2026
Trial IDNCT07720674 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years and older with PTSD symptoms (PCL-5 score ≥ 30) who can commit to 12 weekly sessions and complete all study questionnaires.

Probably not a fit

Individuals with PTSD who do not respond to SEE FAR CBT or who have conditions preventing full participation may not experience benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study uses a single-arm design to deliver SEE FAR CBT over 12 weekly sessions to adults with PTSD. Participants complete self-report questionnaires at baseline, after the intervention, and at a 3-month follow-up to track changes in PTSD symptoms and related psychological outcomes. The study aims to observe how PTSD symptoms evolve during treatment and afterward in a real-world clinical setting. Eligible participants are adults with a PCL-5 score of 30 or higher and who can commit to all study visits and consent procedures. Exclusion criteria include current pregnancy, recent psychotherapy initiation within the last 3 months, or recent initiation of psychiatric medication within 3 months.

Why it matters

Potential benefit: If successful, participants could experience reductions in PTSD symptoms and improvements in related psychological outcomes after completing SEE FAR CBT.

How similar studies have gone: Previous research on trauma-focused CBT approaches in PTSD has shown benefit; this study tests SEE FAR CBT in a single-arm format to establish feasibility and signal of effect.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria

Participants must meet all of the following criteria:

* Age 18 years or older
* PTSD symptoms, defined as a PCL-5 score of 30 or above
* Able to provide informed consent
* Willing and able to participate in 12 weekly individual therapy sessions and complete study questionnaires at baseline, post-intervention, and 3-month follow-up Exclusion Criteria

Participants will be excluded if they meet any of the following criteria:

* Pregnancy at the time of enrollment, due to the potential influence of pregnancy and childbirth during the treatment or follow-up period on psychological outcomes.
* Currently receiving psychotherapy of any type that began less than 3 months prior to enrolment.
* Initiation of psychiatric medication less than 3 months prior to enrolment.

Where it's running

  • Community Stress Prevention Center
    Kiryat Shmona, Israel
    Recruiting

Study contacts

  • Principal investigator: Meital Mashash, PhD — Community Stress Prevention Center
  • Study coordinator: Meital Mashash, PhD
  • Email: meitalm@icspc.org
  • Phone: 972-50-2888052

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.