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Trauma-informed Cognitive Behavioural Therapy (TiCBT) to Aid Reintegration of Repentant Terrorists and Their Families in Nigeria: A Pilot Study

Trauma-informed Cognitive Behavioural Therapy (TiCBT) to Aid Reintegration of Repentant Terrorists and Their Families in Nigeria: A Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05449353
Enrollment
24
Registered
2022-07-08
Start date
2022-07-31
Completion date
2023-06-30
Last updated
2022-07-08

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

Conditions

Psychological, Trauma

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.

Detailed description

The study will adopt a mixed-method single-arm experimental design. Approximately 24 participants will be recruited for the intervention. The Trauma-informed Cognitive Behaviour Therapy (TiCBT) is an 8-session intervention lasting approximately 1 hour each and designed to address trauma, dispel negative attitudes and encourage positive behaviour towards repentant terrorists. Measurement will be collected at baseline pre-intervention, end of intervention and three months post-intervention to determine its feasibility and effectiveness. Interviews will also be conducted post-intervention. Repeated-measures univariate analyses of variance (ANOVA) will be performed to examine differences between the pre- and post-intervention stages. Interviews will be analysed using thematic analysis.

Interventions

BEHAVIORALTrauma-informed Cognitive Behaviour Therapy (TiCBT)

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.

Sponsors

British International Studies Association
CollaboratorUNKNOWN
Tarela Ike
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Patient Health QuestionnaireChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-interventionChange in depression is being assessed
brief Verona Service Satisfaction ScaleChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-interventionChange in service satisfaction is being assessed
Attitude Towards Repentant Terrorists and their Reintegration ScaleChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-interventionChange in of attitude towards repentant terrorists is being assessed
Trauma Screening QuestionnaireChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months post-interventionChange in traumatic experience is being assessed

Contacts

Primary ContactTarela Ike, PhD
t.ike@tees.ac.uk07831163474
Backup ContactDung Jidong, PhD
dung.jidong@ntu.ca.uk07831163474

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026