ClinicalTrials.gg
Status unknownNCT05324670Updated Apr 22, 2022

Title: "Intervention Based on Didactic Model for Suicidal Behavior in the Framework of Impulsivity and Ideations."

An interventional study of Didactic model for suicidal behavior in the framework of impulsivity and ideations in Suicidal Ideation and Behavior and Impulsivity, sponsored by International Islamic University, Islamabad. Status unknown at 1 site in Pakistan. Open to male participants aged 12 Years to 25 Years. Per ClinicalTrials.gov, last updated 2022-04-22.

Sponsored by International Islamic University, Islamabad · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Aug 2021, registered Apr 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
12 Years to 25 Years
Sex
Male
01

Study summary

Suicide has become a major public health problem among young people around the world. This study will examine the effects of higher secondary school-based suicide prevention (HSSSP) program on youth suicidal thoughts and impulsive behavior (STIB). Therefore, the purpose of this study is to examine the effects of didactic approach for youth STIB on the HSSSP program.

This study is designed to address this issue at the secondary school level. Therefore, this research is divided into two studies. In the first study, our goal was to arrange a Baseline assessment for the screening process of adolescents at risk of suicide. while in second study we aim to implement a didactic approach based on religious teachings and culture milieu and examine its effects as an evidence based suicide prevention program.

Read the detailed description

Suicide has become a major public health problem around the world. according to a recent report by the World Health Organization (WHO) suicide is the fourth leading cause of death among youth. Suicidal thoughts and suicide attempts are on the rise among youth. Therefore, evidence-based prevention programs need to fill this gap with interventions at the higher secondary schools.

For decades, research and prevention efforts have been failed in developing meaningful predictions and reductions in suicide. However, significant efforts are needed to stop the rising tide of suicide. For the purpose, it is important to understand the suicidal thought at first as not everyone who commits suicide attempts suicide first.

Therefore, in this study an attempt has been made to investigate profoundly the understanding of suicide which has been emerged a serious problem around the globe and in particular in Pakistani society. The researcher has planned to conduct psychological measures with established psychometric properties to look at the relationship between suicidal ideation and impulsivity anticipating suicidal behavior. During study the role of moderators i.e. social effectiveness and level of religiosity shall also be investigated. Findings of this study shall comprehensively provide data in order to design an inclusive prophylactic strategy known as didactic intervention to prevent the suicidal act before it occurs. It is expected that this approach grounded on religious teaching and cultural milieu in line with the best practices, will be adapted. Subsequently, this study also aims to evaluate the effectiveness of the didactic approach as an evidence based suicide prevention program in higher secondary schools with selective prevention programs.

02

Conditions studied

  • Suicidal Ideation and Behavior
  • Impulsivity
03

In context

Suicidal Ideation

569 studies on the registry are indexed under Suicidal Ideation; 203 are open to participants now.

This study's planned enrollment of 150 is above the median of 80 across 469 interventional studies indexed under Suicidal Ideation.

Browse Suicidal Ideation studies →

Lead sponsor

International Islamic University, Islamabad is the lead sponsor of 10 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
12 Years to 25 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Higher Secondary School Students
  • Young people at risk of suicide: those who are impulsive and have suicidal thoughts.

Exclusion criteria

Exclusion Criteria:

  • Who has a history of suicide attempts
05

Study design

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

Study arms

  • Experimental
    Experimental condition

    Didactic intervention based on religious teachings and cultural milieu, the experimental group will receive 12 sessions for three months, 4 sessions per month including focused group discussion.

    Other: Didactic model for suicidal behavior in the framework of impulsivity and ideations

  • Other
    Control condition

    They will have sessions like the experimental group but the control group will get the knowledge in the form of written material without any explanation (Information Leaflet).

    Other: Didactic model for suicidal behavior in the framework of impulsivity and ideations

Interventions

  • OtherDidactic model for suicidal behavior in the framework of impulsivity and ideations

    It will be in the form of lectures (Educational approach). Content will be developed one day before the commencement of the session. The Knowledge provided in the form of written material with proper explanation shall not exceed 30 minutes and a Focused group Discussion will be held at the end of each month.

    Also known as: Prophylactic Strategy Known as Didactic intervention

06

What researchers measure

Primary outcomes

  1. Barratt Impulsiveness scale

    This is a 4-point likert scale and is scored in the following way; Rarely/Never= 1, Occasionally= 2, Often= 3 \& Almost/Always= 4. It contains 30 items that describe common impulsive or non-impulsive behaviors and preferences.

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

  2. Beck Scale for Suicidal Ideation

    This scale entails of 19 items and measures 3 responses from Least severe= 0 to Most severe= 2

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

Secondary outcomes

  1. Depression Anxiety Stress Scale (DASS)

    This scale consists of a set of three self-reported measures in the form of 4-point Likert severity/frequency format. Each scale contains 14 items, subdivided into 2-5 item subscales containing the same contents.

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

  2. Stroop Test

    The Stroop Color Test assesses the ability to prevent cognitive interference, which occurs while processing the stimulus feature affects the simultaneous processing of another attribute of the same stimulus.

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

  3. Self-Efficacy scale

    It is a 4-point Likert-type scale consisting of 10 items, and measures are taken in response from strongly disagree to strongly agree.

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

  4. Religious commitment inventory (RCI-10)

    This scale consists of 10 items. The responses are made in a 5 - point Likert format from Not at all to Totally true of me.

    Time frame: Assessment at baseline (after screening), 8th week after baseline (2 months), 16th week after baseline (4 months). The purpose of the outcome measure is to estimate the change from baseline assessment to follow-up.

07

Study locations

1 of 1 sites recruiting
  • International Islamic University
    Islamabad, Islamabad (CapitalTerritory) 44000, Pakistan
    Recruiting
    • Muhammad T Khalily, PhD · Principal investigator
08

References and documents

Publications

  • Eggert LL, Thompson EA, Herting JR, Nicholas LJ. Reducing suicide potential among high-risk youth: tests of a school-based prevention program. Suicide Life Threat Behav. 1995 Summer;25(2):276-96. Erratum In: Suicide Life Threat Behav 1999 Spring;29(1):96. PubMed 7570788 ↗
  • Aseltine RH Jr, DeMartino R. An outcome evaluation of the SOS Suicide Prevention Program. Am J Public Health. 2004 Mar;94(3):446-51. doi: 10.2105/ajph.94.3.446. PubMed 14998812 ↗
  • Randell BP, Eggert LL, Pike KC. Immediate post intervention effects of two brief youth suicide prevention interventions. Suicide Life Threat Behav. 2001 Spring;31(1):41-61. doi: 10.1521/suli.31.1.41.21308. PubMed 11326768 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05324670
Lead sponsor
International Islamic University, Islamabad
Responsible party
Mudassar Abdullah (Mudassar Abdullah, International Islamic University, Islamabad) — Principal investigator
First posted
Apr 12, 2022
Start date
Aug 1, 2021
Primary completion
Jun 1, 2022 (estimated)
Completion
Aug 1, 2022 (estimated)
Last update
Apr 22, 2022

Study contacts

Abdullah
Contact
mkhankhalil@ymail.com
03459149029
Muhammad T Khalily
Contact
dr.khalily@iiu.edu.pk
03475710446
Dr. Muhammad T Khalily
study chair · Department of Psychology, IIUI

Oversight

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

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