Peer-led Group Intervention for Coping With Disaster

PTSD Clinical Trial

Official title:

Peer-led Group Intervention for Coping With Disaster

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03907995
• Other study ID #: H-44353
• Status: Completed
• Phase: N/A
• Start date: May 29, 2019
• Est. completion date: December 31, 2019

Study information

• Verified date: May 2020
• Source: Baylor College of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The present project partners with leading faith communities in Houston to provide expert-led educational workshops to a diverse sample of adults on normative and concerning response to disaster. Secondly implementing peer-led interventions where a trained adult leads others through an evidence-based manualized intervention. Lastly, identifying and referring individuals who require more intensive services to a higher level of care.

Description:

Approximately 20% of individuals have significant behavioral health concerns. Exposure to a disaster like Hurricane Harvey and its aftermath often exacerbates pre-existing issues and/or brings new issues, with post-traumatic stress presenting in manners such as anxiety, depression, conduct issues and/or somatic issues. Approaches are needed that educate community members about both normative and concerning responses to disaster focused on coping skills development. A particular approach, peer-led intervention groups have been shown effective at delivering these types of intervention. Brief, psycho-educational peer-led programs have shown effectiveness in a variety of forums including helping promote adjustment among those who have experienced trauma. There will be six group sessions every two weeks. Sessions will include how to teach appropriate coping techniques to respond to the distress, confronting distressing memories related to the disaster, and emotion regulation techniques. After the group sessions end, individuals who require a more intensive service will be referred to a higher level of care.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: December 31, 2019
• Est. primary completion date: December 31, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years and older and English speaking.

Exclusion Criteria:

• Individuals under the age of 18 and non-English speaking and participants who do not wish to participate in this study.

Related Conditions & MeSH terms

• Anger
• Anxiety Disorder
• Anxiety Disorders
• Depression
• Depressive Disorder
• Depressive Symptoms
• Disease
• PTSD

Intervention

Behavioral:
• Cognitive Behavioral Therapy
The form of treatment will involve 6 group sessions every two weeks about an hour each. Sessions consist of teaching a different coping technique in each session to help cope with disaster or other events.

Locations

Country	Name	City	State
United States	Baylor College of Medicine: Jamail Specialty Care Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Baylor College of Medicine	American National Red Cross

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PTSD Symptom Scale - Adult	The PTSD Symptom Scale - Self Report is a 17-item, Likert-scale, self-report questionnaire designed to assess the symptoms of PTSD according to DSM-IV. Each of the 17 items is rated on a scale from 0 to 3, with total score ranging from 0 to 51 by adding them up.	Post-treatment, which is 12 weeks after baseline.