NCT07627451

Brief Summary

Mental health difficulties among males are an issue of public health concern. Men are also at higher risk of suicidal ideation and self-harm and are poor at help-seeking due to factors including stigma, cultural norms and gendered expectations of masculinity. Yet, in Nigeria, a significant gap remains in media orientation intervention to create awareness on symptoms of mental health difficulties and support channels to encourage help-seeking. In essence, the current study aims to test the feasibility and acceptability of a novel intervention titled, psyChosOcial media awareNesS for SuiCIde symptoms, including other mental health PrOblems and help seeking mediUmS (CONSCIOUS) for addressing awareness of mental health difficulties in comparison to the waitlist control group for the purposes of improving men's help seeking, social support and reducing anxiety in Nigeria.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P25-P50 for not_applicable anxiety

Timeline
11mo left

Started Jun 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 30, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 4, 2026

Completed
26 days until next milestone

Study Start

First participant enrolled

June 30, 2026

Expected
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 3, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 3, 2027

Last Updated

June 4, 2026

Status Verified

May 1, 2026

Enrollment Period

11 months

First QC Date

May 30, 2026

Last Update Submit

May 30, 2026

Conditions

Keywords

Help-seeking for mental health difficultiessuicidal ideationself harm awarenessmedia awareness for mental health difficulties

Outcome Measures

Primary Outcomes (1)

  • Service Satisfaction Scale

    A five item scale that can be used to assess and measure satisfaction, acceptability and quality of the intervention. Higher score denote positive outcomes and acceptability. Lower score denotes poor satisfaction and acceptability.

    Immediately after the end of the intervention

Secondary Outcomes (10)

  • Generalised Anxiety Disorder (GAD-7)

    Baseline (day 1) and at the end of intervention (day 2)

  • Attitude Towards Seeking Professional Psychological Help Scale

    Baseline (day 1) and at the end of intervention (day 2)

  • General Help Seeking Questionnaire (GHSQ)

    Baseline (day 1) and at the end of intervention (day 2)

  • Self Stigma and Help Seeking (SSHS) Scale

    Baseline (day 1) and at the end of intervention (day 2)

  • Stigma of Suicide Scale (SOSS)

    Baseline (day 1) and at the end of intervention (day 2)

  • +5 more secondary outcomes

Study Arms (2)

Experimental : psyChosOcial media awareNesS for SuiCIde symptoms and other mental health PrOblems

EXPERIMENTAL

Low intensity media campaign intervention

Behavioral: Psychosocial media campaign

Control - Intervention as Usual/Waitlist

OTHER

Intervention as Usual / Waitlist to be administered the CONSCIOUS intervention after assessment at baseline (day 1) and end of intervention (day 2).

Other: Intervention as usual

Interventions

The CONSCIOUS is 3 minutes recorded media message. The intervention is designed to promote awareness on how to prevent suicidal ideation and self-harm, stigma reduction and avenues or mediums for help-seeking. The core message is composed of three key ambits: 1) emphasizing what is meant by suicidal ideation and self-harm (ii) the need to seek help and stop societal stigmatising behaviour (iii) Avenues for help seeking and improved mental health and wellbeing.

Experimental : psyChosOcial media awareNesS for SuiCIde symptoms and other mental health PrOblems

Current available interventions to foster help seeking including leaflets, community health centre provision of information etc. This group will be later offered the CONSCIOUS intervention after completion of baseline and end of intervention assessment.

Control - Intervention as Usual/Waitlist

Eligibility Criteria

Age18 Years+
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsMale aged 18 years and above.
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • male, aged 18 years or above, able to provide full informed consent to aid their participation, able to speak the English language which is Nigeria language. able to take part in the intervention and are available for the intervention assessment at baseline and end of intervention.

You may not qualify if:

  • less than 18 years old, unable to provide informed consent, undergoing severe mental health treatment and unable to speak the English language. Participants were also excluded if they are high risk social ideation or self-harm patients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Pirkis J, Rossetto A, Nicholas A, Ftanou M, Robinson J, Reavley N. Suicide Prevention Media Campaigns: A Systematic Literature Review. Health Commun. 2019 Apr;34(4):402-414. doi: 10.1080/10410236.2017.1405484. Epub 2017 Nov 30.

    PMID: 29190128BACKGROUND
  • Ftanou M, Cox G, Nicholas A, Spittal MJ, Machlin A, Robinson J, Pirkis J. Suicide Prevention Public Service Announcements (PSAs): Examples from Around the World. Health Commun. 2017 Apr;32(4):493-501. doi: 10.1080/10410236.2016.1140269. Epub 2016 Jun 16.

    PMID: 27308843BACKGROUND

MeSH Terms

Conditions

Anxiety DisordersPsychological Well-BeingSuicide PreventionSuicidal Ideation

Interventions

Methods

Condition Hierarchy (Ancestors)

Mental DisordersPersonal SatisfactionBehaviorSuicideSelf-Injurious BehaviorBehavioral Symptoms

Intervention Hierarchy (Ancestors)

Investigative Techniques

Central Study Contacts

Tarela J Ike, PhD

CONTACT

Dung E Jidong, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Lecturer/ Principal Investigator

Study Record Dates

First Submitted

May 30, 2026

First Posted

June 4, 2026

Study Start (Estimated)

June 30, 2026

Primary Completion (Estimated)

June 3, 2027

Study Completion (Estimated)

June 3, 2027

Last Updated

June 4, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Data supporting this study cannot be made available due to the sensitive nature and ethical reasons on confidentiality.