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The effectiveness of rational emotive behavior therapy (REBT) intervention on post-traumatic stress syndrome management in pre-hospital emergency personnel

The effectiveness of rational emotive behavior therapy (REBT) intervention on post-traumatic stress syndrome management in pre-hospital emergency personnel

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260108068596N1
Enrollment
112
Registered
2026-04-15
Start date
2026-02-27
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Traumatic Stress Syndrome.

Interventions

Intervention group: The study includes an intervention group that will receive Rational Emotive Behavior Therapy (REBT) over the course of 8 sessions..

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Holding a bachelor’s or master’s degree in nursing, and an associate’s or bachelor’s degree in Emergency Medical Services, and an associate’s or bachelor’s degree in Operating Room and Anesthesia, Working as one of the technician cadres (Emergency Medical Technician [EMT], Basic Technician, Intermediate Technician, or Senior Technician) in the Pre-hospital Emergency Medical Center, Working at Pre-hospital Emergency Medical Services (EMS 115) as the primary occupation, Employed exclusively in the operational units of the Pre-hospital Emergency Medical Center, Achieve a minimum score of 24 on the IES-R scale.

Exclusion criteria

Exclusion criteria: A known case of psychotic disorders based on self-report and staff health records, having a history of treatment for post-traumatic stress disorder and participation in cognitive-behavioral therapy or its variants, and rational-emotive behavior therapy interventions based on self-report; absence from more than one therapy session; incomplete completion of data-collection instruments; failure to regularly perform intervention exercises; transfer or death of the technician

Design outcomes

Primary

MeasureTime frame
Post-Traumatic Stress Syndrome. Timepoint: Measurement of post-traumatic stress disorder (PTSD) will be conducted at the beginning of the study and then sequentially at 4, 8, and 12 weeks after the implementation of the intervention. Method of measurement: The Impact of Event Scale - Revised (IES-R).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Rezai

Shahroud University of Medical Sciences

S.Rezaei@shmu.ac.ir+98 23 3239 5054

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026