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A study of the effectiveness of transdiagnostic unified protocol on the treatment of posttraumatic stress disorder

A study of the effectiveness of transdiagnostic unified protocol on the treatment of posttraumatic stress disorder and comorbid symptoms in survivors of earthquake

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180421039369N4
Enrollment
33
Registered
2019-12-13
Start date
2019-06-22
Completion date
Unknown
Last updated
2019-12-17

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

Conditions

Post Traumatic Stress Disorder.

Interventions

Intervention 1: Intervention group: In this study, Barlow's integrated, meta-diagnostic ultrasound treatment will be used. The sample included 33 individuals, divided randomly into two groups of exper

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Minimum age 18 and maximum 40 yesrs Minimum tertiary guidance education a person with post-traumatic stress disorder trauma after experiencing sarpole zahab earthquake as a diagnosis based on a psychologist Motivation and lack of motivation to participate in treatment No symptoms of disassociation.

Exclusion criteria

Exclusion criteria: Criteria exit :Psychotic and bipolar disorder, uncontrollable flashback

Design outcomes

Primary

MeasureTime frame
Posttraumatic stress disorder. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: Mississippi Scale.

Secondary

MeasureTime frame
Depression. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: Beck Depression Inventory(BDI-II).;Anxiety. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: ,Hamiton Rating Scale for Anxiety(HRSA).;Quality of Life. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: Ware & Sherbourne Inventory,.;Sleep Quality. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: ,Pittsburgh Sleep Quality Index.;Posttraumatic stress disorder. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: Mississippi Scale.;Social Adjustment. Timepoint: A week befor the intervention,one week after the intervention,Two months after the intervention. Method of measurement: Bell Adjustment Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid piri

Kermanshah University of Medical Sciences

nahidpiri1989@gmail.com+98 83 3827 2949

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026