NCT05449353

Brief Summary

The aim of the study is to describe the feasibility, cultural appropriateness, and acceptability of Trauma-informed Cognitive Behaviour Therapy (TiCBT) to promote community healing and encourage the reintegration of repentant terrorists and their families to avoid reoffending.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2022

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 4, 2022

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 8, 2022

Completed
23 days until next milestone

Study Start

First participant enrolled

July 31, 2022

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2023

Completed
Last Updated

July 8, 2022

Status Verified

July 1, 2022

Enrollment Period

10 months

First QC Date

July 4, 2022

Last Update Submit

July 4, 2022

Conditions

Outcome Measures

Primary Outcomes (4)

  • Trauma Screening Questionnaire

    Change in traumatic experience is being assessed

    Change is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-intervention

  • Patient Health Questionnaire

    Change in depression is being assessed

    Change is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-intervention

  • Attitude Towards Repentant Terrorists and their Reintegration Scale

    Change in of attitude towards repentant terrorists is being assessed

    Change is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-intervention

  • brief Verona Service Satisfaction Scale

    Change in service satisfaction is being assessed

    Change is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-intervention

Study Arms (1)

Trauma-infomed Cognitive Behavioural Therapy

EXPERIMENTAL

Experimental (n=24 participants) will receive the TiCBT which consists of a total of 8-group integrated sessions lasting approximately 60 minutes per session every 3 days interval with 24 persons in the single group.

Behavioral: Trauma-informed Cognitive Behaviour Therapy (TiCBT)

Interventions

Group: Experimental (n=24 participants) will receive the TiCBT which consists of a total of 8-group integrated sessions lasting approximately 60 minutes per session every 3 days interval with 24 persons in the single group.

Trauma-infomed Cognitive Behavioural Therapy

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • community members who are victims of Boko Haram terrorism and had previous experiences of trauma/depression,
  • score five and above for the culturally-adapted Trauma Screening Questionnaire (Brewinn et al., 2002)
  • aged 18+ years,
  • able to give informed consent,
  • speak English
  • are residents or from areas within Nigeria including Maiduguri, Adamawa, and Plateau environs.

You may not qualify if:

  • less than 18 or above 85 years
  • unable to give consent
  • clinically diagnosed with severe PTSD/suicidal ideations or undergoing treatment
  • temporary or non-residents who are unlikely to be available for follow up

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Wounds and Injuries

Central Study Contacts

Tarela Ike, PhD

CONTACT

Dung Jidong, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

July 4, 2022

First Posted

July 8, 2022

Study Start

July 31, 2022

Primary Completion

May 30, 2023

Study Completion

June 30, 2023

Last Updated

July 8, 2022

Record last verified: 2022-07

Data Sharing

IPD Sharing
Will not share