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CaMaPi for Adolescents/Young People With a History of Self-harm and Suicidal Ideation in Jos, Nigeria

Culturally-adapted Manual-assisted Psychological Intervention (CaMaPi) for Adolescents/Young People With a History of Self-harm and Suicidal Ideation in Jos, Nigeria

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06440031
Acronym
CaMaPi
Enrollment
32
Registered
2024-06-03
Start date
2024-07-01
Completion date
2025-09-30
Last updated
2024-06-03

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

Conditions

Self-harm, Suicidal Ideation

Brief summary

Suicide and self-harm are global disease burden that contributes significantly to years of lost life and mortality.

Detailed description

Self-harm and suicidal ideation represent a significant global public health concern (Knipe et al., 2022), affecting about 14.6 million people yearly (Nichols et al., 2021). Globally, over 700 000 people die by suicide annually (World Health Organization -- WHO, 2023). Suicide is the fourth leading cause of death among 15-29-year-olds, and 77% of global suicides occur in low- and middle-income countries, including Nigeria (WHO, 2023). The psychological impact of suicidal ideation includes continuing high tendencies of self-harm (Jidong et al., 2024). Despite the increasing rates of suicide and self-harm in Nigeria, this topic is understudied, with no culturally appropriate or sustainable psychological interventions.

Interventions

BEHAVIORALCaMaPi

CaMaPi is a manually assisted brief psychological intervention that is based on the principles of Cognitive Behaviour Therapy (CBT). The intervention includes psycho-education and a comprehensive cognitive behavioural assessment of the suicidal ideation and self-harm attempt using virtual stories of four young people to be delivered in 8-10 sessions for over three months

OTHERTAU

Treatment as Usual (TAU) is routine care, such as diagnosis, assessment, psychotherapy, monitoring and any form of intervention (e.g., medication prescription) available at the collaborating service.

Sponsors

University of Manchester
CollaboratorOTHER
Jos University Teaching Hospital
CollaboratorOTHER
Teesside University
CollaboratorOTHER
Nottingham Trent University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
16 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients aged 16-24 years presenting to the participating services, and emergency departments or admitted after an episode of self-harm to the participating hospitals or self-referrals. * Participants will have to be living within the catchment area of the participating practices, services and hospitals. * Not needing inpatient psychiatric treatment.

Exclusion criteria

* Severe mental illness (such as Psychotic disorder). * Conditions limiting engagement with assessment/intervention. * Temporary resident unlikely to be available for follow up.

Design outcomes

Primary

MeasureTime frameDescription
Change in acceptance and satisfaction with the interventionChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionPrimary outcome measure would be assessed using the Service Satisfaction Scale

Secondary

MeasureTime frameDescription
Change in hopelessnessChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using the Beck Hopelessness Scale
Change in Health StatusChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using the EQ-5D-5L quality of health scale
Change in suicidal ideationChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using the Beck Scale for Suicide Ideation
Change in use of health servicesChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using Client Service Receipt Inventory
Change in psychological distressChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using Kessler Psychological Distress Scale
Change in repetition rate's of self-harmChange is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-interventionSecondary outcome measure would be assessed using an adapted Suicide Attempt Self-Injury Interview

Contacts

Primary ContactDung Jidong, PhD
dung.jidong@mamnchester.ac.uk07448930519

Outcome results

None listed

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