CClinicalTrials.gg
Not yet recruitingNCT06440031CaMaPiUpdated Jun 3, 2024

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

An interventional study of CaMaPi and TAU in Self-harm and Suicidal Ideation, sponsored by Nottingham Trent University. Not yet recruiting. Open to participants aged 16 Years to 24 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-06-03.

Sponsored by Nottingham Trent University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
16 Years to 24 Years
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Self-harm
  • Suicidal Ideation
03

In context

Suicidal Ideation

515 studies on the registry are indexed under Suicidal Ideation; 195 are open to participants now.

This study's planned enrollment of 32 is below the median of 80 across 426 interventional studies indexed under Suicidal Ideation.

Browse Suicidal Ideation studies →

Lead sponsor

Nottingham Trent University is the lead sponsor of 28 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 24 Years
Sexes eligible
All
Accepts 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

Exclusion Criteria:

  • Severe mental illness (such as Psychotic disorder).
  • Conditions limiting engagement with assessment/intervention.
  • Temporary resident unlikely to be available for follow up.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
32 participants (estimated)

Study arms

  • Experimental
    CaMaPi

    Behavioral: CaMaPi

  • Active comparator
    TAU

    Other: TAU

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.

06

What researchers measure

Primary outcomes

  1. Change in acceptance and satisfaction with the intervention

    Primary outcome measure would be assessed using the Service Satisfaction Scale

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

Secondary outcomes

  1. Change in suicidal ideation

    Secondary outcome measure would be assessed using the Beck Scale for Suicide Ideation

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

  2. Change in hopelessness

    Secondary outcome measure would be assessed using the Beck Hopelessness Scale

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

  3. Change in Health Status

    Secondary outcome measure would be assessed using the EQ-5D-5L quality of health scale

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

  4. Change in repetition rate's of self-harm

    Secondary outcome measure would be assessed using an adapted Suicide Attempt Self-Injury Interview

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

  5. Change in use of health services

    Secondary outcome measure would be assessed using Client Service Receipt Inventory

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

  6. Change in psychological distress

    Secondary outcome measure would be assessed using Kessler Psychological Distress Scale

    Time frame: Change is being assessed from baseline, end of intervention at 12 weeks, and at 12 weeks post-intervention

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06440031
Lead sponsor
Nottingham Trent University
Collaborators
University of Manchester, Jos University Teaching Hospital, Teesside University
Responsible party
Dr Dung Jidong, PhD (Dr, Nottingham Trent University) — Principal investigator
First posted
Jun 3, 2024
Start date
Jul 1, 2024 (estimated)
Primary completion
Jun 30, 2025 (estimated)
Completion
Sep 30, 2025 (estimated)
Last update
Jun 3, 2024

Study contacts

Dung Jidong, PhD
Contact
dung.jidong@mamnchester.ac.uk
07448930519 ext. +44

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion