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Suicide Ideation Intervention in Nigeria

Primary Purpose

Suicide

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Comprehensive SEM-Based Program
Sponsored by
Babcock University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Suicide

Eligibility Criteria

10 Years - 19 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Duly enrolled students
  • Aged 10-19 years
  • No plans of leaving the school in the next year
  • Give consent
  • Parental/guardians' assent

Exclusion Criteria:

  • Nil

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Intervention

    Control

    Arm Description

    Comprehensive theory-based suicide behavior program

    No intervention will be given to the group

    Outcomes

    Primary Outcome Measures

    Suicide Ideation
    Adolescent Suicide Ideation measured using the Positive and Negative Suicide Ideation (PANSI) Inventory. The scores range from six to thirty for PANSI-Positive Inventory (PI) and eight to 40 for PANSI-Negative Suicide Inventory (NSI). Higher scores on PANSI-NSI scale and lower marks on PANSI-PI) symbolize the higher frequency of suicidal thoughts.

    Secondary Outcome Measures

    Gratitude
    Measured with the Gratitude Questionnaire. The aggregate score should be between six to 42. Participants scoring less than the 50th percentile (38) are low in gratitude.
    Grit
    Measured with the Grit scale. The maximum aggregate is five (extremely gritty), and the minimum score is one (not at all gritty).
    Mental Health Status
    Measured with the General Health Questionnaire (GHQ-12). The obtainable scores range from 0 to 36. Scores less than12 suggest the absence of distress.

    Full Information

    First Posted
    October 21, 2021
    Last Updated
    February 6, 2023
    Sponsor
    Babcock University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05103540
    Brief Title
    Suicide Ideation Intervention in Nigeria
    Official Title
    Patterns and Risk Factors for Suicide Ideation Among In-school Adolescents in Nigeria and a Comprehensive Suicide-behavior Prevention Intervention Pilot Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    July 2023 (Anticipated)
    Primary Completion Date
    June 2025 (Anticipated)
    Study Completion Date
    June 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Babcock University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The research will use the Social Ecologic Model of behavior and WHO mhGAP framework to design a comprehensive intervention across three levels (individual, interpersonal, and social) of influence. The study will then pilot the intervention in 15 secondary schools through a Stepped-Wedge Cluster-Randomized trial. After screening for eligibility and selecting participating schools and individuals, investigators will randomize at the cluster level and switch the groups from control to intervention arms at three months' intervals till the research has moved all the clusters. The study will collect data at baseline, the switch points, and the end of the study. The goal is to evaluate the feasibility, effectiveness of a comprehensive suicide behavior prevention intervention among in-school adolescents in Nigeria. Another aim is to identify barriers and facilitators of implementation and the best practices for scaling up the intervention. It is hypothesized that because our intervention is based on the best contextual evidence and built on a sound theoretical model, it will successfully mitigate suicide ideation. Also, the nature and efficiency of the stepped wedge cluster randomized design will enhance the feasibility in the local context, characterized by political, logistic, and ethical constraints.
    Detailed Description
    The effect of comprehensive suicide behavior prevention intervention among in-school adolescents Nigeria: a stepped-wedge cluster randomized trial This study aims to evaluate the feasibility and effectiveness of a theory-based comprehensive suicide behavior prevention intervention among in-school adolescents in the Ikenne local government area (LGA) of Ogun State, Nigeria. The methodology of the study is a Stepped-wedge cluster-randomized trial of a suicide behavior intervention among fifteen secondary schools in Nigeria. The study chose the stepped-wedge design because although the investigators expect the intervention to reduce suicidal ideation, the feasibility of a full implementation may be challenging due to political, logistical, and ethical constraints. The design fulfills a secondary role of serving as a scientific tool to incorporate a fair method to determine the order of intervention rollout under logistic impediments. The implementation of our intervention is feasible only at the cluster level. Investigators will conduct a Stepped-Wedge Cluster Randomized Trail among 15 secondary schools over one year. The participating schools will cross in a one-way switch over from the control to the intervention period. The sequence of switch over for the clusters will follow a stratified randomization scheme. All the schools will receive the intervention by the end of the study. All the groups will be recruited at the study onset and will act as control until the point of randomization into the intervention group. To mitigate contamination, the study will provide clear information on the purpose of the research to the participants. The clusters will get the details of intervention at the point of switching into the experimental group. The study will educate the intervention group against contamination. Also, the investigators will assess the exposure of the control group to the intervention before switching them. The study will report the level of contamination. The study will recruit 15 secondary schools with a minimum of 100 enrolled students and do not have an existing suicide behavior intervention program. The school boards need to approve participation. Eligible students should be aged 10-19 years, give consent, and not have plans of leaving the school in the next year. Parental/guardians' assent is also a prerequisite for participation in the study. The study will not exclude non-participating students from the delivery of the intervention. The study will randomly select, by balloting, Five (three publicly and two privately-owned) schools in each of the three areas of the LGA. The selection of students will follow a probability sampling method. Eligible schools will be randomized into three sequences of five schools each, using a computer-generated stratified randomized sampling scheme. The stratification, which will be according to the area and ownership of the schools, will be supervised by the PIs. The nature of the experiment and intervention makes blinding unrealistic. However, investigators will ensure the conduct of the measurement of the study outcome objectively. The intervention is a four-pronged comprehensive suicidal behavior prevention intervention in schools. The prongs consist of evidence-based interventions that use the Social Ecological Model (SEM). The SEM theorizes that there are multiple inter-related levels of influences on human behavior, and a successful preventive program should address factors at each stratum. The intervention addresses three levels; individual, interpersonal, and social. Firstly, the research will collaborate with relevant stakeholders to design and obtain a commitment from the schools to a suicidal behavior prevention policy and protocol document. Secondly, the intervention will train staff and students on best practices to improve students' connectedness thereby, creating a positive school environment. Thirdly, the study will identify and train gatekeepers on the proper response to suicidal thoughts and other suicidal behaviors; and serve as the link between the students and a school-linked mental health specialist. The research will train the gatekeepers to use school-based screening tools. Lastly, this research will educate all students on suicidal behaviors. This prong will create awareness, promote case-finding, and provide information about available mental health resources. Also, the intervention will address the stereotypes that promote stigma and improve the students' coping abilities. The entire intervention will incorporate peer support and student involvement at all stages of planning and implementation. The primary outcome is suicidal ideation, as assessed by the Positive Inventory of the Positive and negative Suicide Ideation (PANSI-PI). PANSI is a 14-item scale consisting of two subscales, the 6-item positive scale (PANSI-PI) and the 8-item negative (PANSI-NSA). Higher scores on PANSI-NSI scale and lower marks on PANSI-PI) symbolize the higher frequency of suicidal thoughts. The secondary outcomes are grit, gratitude, and mental health status. The study will use the gratitude questionnaire(GQ-6), the grit scales, and the General Health Questionnaire (GHQ-12) to assess gratitude, determination, and mental health status, respectively. The sample size was determined using the Shiny CRT Calculator, a power and sample size tool for cluster-randomized trials. The aim was to have three sequences with five clusters each, assuming an intra-cluster correlation coefficient of 0.01 (0 to 0.02) and individual autocorrelation of 0.08. The study desires a minimum statistical power of at least 90%, considering a type I error of 5% and a 10% increase in the mean PANSI-PI score from 17.71 (_6:35) attributable to the intervention. Some allowance will be made for a school dropout rate of 23.12%. The derived sample size was 30 per cluster. The study will analyze the data using Stata/SE 15.1 statistical software. The statistical analysis is rooted in the principle of intention-to-treat and will use random effect mixed modeling to address missing data while assuming that missingness is at random. The research will use the linear mixed model for continuous outcomes and the generalized linear mixed model for categorical outcomes and adjust for the possible confounding effects of individual-level characteristics that our randomization did not capture. Also, the study will adjust for age, sex, number of years in the school, ethnicity, and secular trends (the school term), and will use multilevel analysis to adjust for cluster effect and the correlation between repeated measurements. The expected outcome of the research includes a suicidal behavior prevention policy and protocol template for secondary schools in Nigeria and an effective suicide behavior prevention program that is scalable for Ogun State, Nigeria.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Suicide

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    450 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Comprehensive theory-based suicide behavior program
    Arm Title
    Control
    Arm Type
    No Intervention
    Arm Description
    No intervention will be given to the group
    Intervention Type
    Behavioral
    Intervention Name(s)
    Comprehensive SEM-Based Program
    Intervention Description
    The SEM theorizes that there are multiple inter-related levels of influences on human behavior, and a successful preventive program should address factors at each stratum. My intervention addresses three levels; individual, interpersonal, and social. Firstly, the research will collaborate with relevant stakeholders to design and obtain a commitment from the schools to a suicidal behavior prevention policy and protocol document. Secondly, the intervention will train staff and students on best practices to improve students' connectedness thereby, creating a positive school environment. Thirdly, the study will identify and train gatekeepers on the proper response to suicidal thoughts and other suicidal behaviors; and serve as the link between the students and a school-linked mental health specialist. We will train the gatekeepers to use school-based screening tools. Lastly, this research will educate all students on suicidal behaviors.
    Primary Outcome Measure Information:
    Title
    Suicide Ideation
    Description
    Adolescent Suicide Ideation measured using the Positive and Negative Suicide Ideation (PANSI) Inventory. The scores range from six to thirty for PANSI-Positive Inventory (PI) and eight to 40 for PANSI-Negative Suicide Inventory (NSI). Higher scores on PANSI-NSI scale and lower marks on PANSI-PI) symbolize the higher frequency of suicidal thoughts.
    Time Frame
    12 weeks
    Secondary Outcome Measure Information:
    Title
    Gratitude
    Description
    Measured with the Gratitude Questionnaire. The aggregate score should be between six to 42. Participants scoring less than the 50th percentile (38) are low in gratitude.
    Time Frame
    12 weeks
    Title
    Grit
    Description
    Measured with the Grit scale. The maximum aggregate is five (extremely gritty), and the minimum score is one (not at all gritty).
    Time Frame
    12 weeks
    Title
    Mental Health Status
    Description
    Measured with the General Health Questionnaire (GHQ-12). The obtainable scores range from 0 to 36. Scores less than12 suggest the absence of distress.
    Time Frame
    12 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    10 Years
    Maximum Age & Unit of Time
    19 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Duly enrolled students Aged 10-19 years No plans of leaving the school in the next year Give consent Parental/guardians' assent Exclusion Criteria: Nil
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Olumide Abiodun
    Phone
    +2347038569725
    Email
    abioduno@babcock.edu.ng
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Olumide Abiodun
    Organizational Affiliation
    Babcock University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    All study data will be de-identified

    Learn more about this trial

    Suicide Ideation Intervention in Nigeria

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