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Clinical Trials/NCT06159075
NCT06159075
Completed
Not Applicable

Reducing Self-Stigma Among Individuals with History of Childhood Maltreatment: a Cross-Cultural Lens

Research Foundation for Mental Hygiene, Inc.1 site in 1 country964 target enrollmentJanuary 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stigma, Social
Sponsor
Research Foundation for Mental Hygiene, Inc.
Enrollment
964
Locations
1
Primary Endpoint
Self-Stigma Questionnaire - Follow-Up
Status
Completed
Last Updated
last year

Overview

Brief Summary

Individuals who report experiencing any kind of abuse during childhood report shame and self-blame, often leading to self-stigma and a reluctance to reveal their experiences and seek help. Such stigma may aggravate the mental health consequences of child maltreatment (CM).

The investigators hypothesize that:

  1. The brief video-based intervention will have the immediate and repeated effect of reducing self-stigma among CM survivors compared with the control condition.
  2. The brief video-based intervention will increase seeking treatment compared with the control condition.
  3. The brief video-based intervention will show similar effects in reducing self-stigma across multiple countries.

Detailed Description

Prior research suggests that social contact-based interventions are the most efficient way of reducing stigma. This study aims to address self-stigma and empower individuals who self-reported experiencing any kind of abuse during childhood and increase their openness to seeking help, if needed. Four hundred participants with self-reported experience of any kind of childhood abuse will be recruited to participate in a Randomized Controlled Trial (RCT) testing the efficacy of the intervention. Participants will be randomized into one of two arms: 1) A 2-minute video intervention in which a CM survivor (presented by an actor) shares their personal CM experience and describes how they were able to overcome feelings of shame and self-blame to seek mental health care; or 2) A 2-minute control video using the same actor, but without a personal narrative of CM experience. Both videos will be preceded by and immediately followed by questionnaires assessing self-stigma and openness to seeking treatment. An additional assessment of emotional engagement will be added immediately following intervention delivery. Following the intervention, there will be a 30- day follow-up to examine potential long-term effects. The results will be analyzed alongside results from parallel protocols being conducted by partner sites in other countries (Switzerland, Sweden, Japan, Peru, India, Australia, Turkey, South Africa, and Israel). Each site will conduct the study under their own university's purview and with their own protocol, and only deidentified data will be shared for analysis. All study procedures will be conducted remotely via CloudReseach and Mechanical Turk, which is a crowdsourcing platform. The study survey will be hosted by Qualtrics.

Registry
clinicaltrials.gov
Start Date
January 1, 2024
End Date
April 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yuval Y Neria

Professor, and Director of PTSD at Columbia University

Research Foundation for Mental Hygiene, Inc.

Eligibility Criteria

Inclusion Criteria

  • Age 18-80
  • US resident
  • Individuals who endorse yes to one of the following items: physical aggression in family or household, emotional or verbal abuse in family or household, sexual abuse or inappropriate sexual experiences, negligence - physical or emotional, mental illness or substance abuse at home, incarceration of family member
  • Fluent in English and able to give informed consent

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Self-Stigma Questionnaire - Follow-Up

Time Frame: 30 days post-intervention

Change in stigma items from baseline - higher score indicates higher stigma (range of 15 to 60)

Help Seeking Intentions - Post-Intervention

Time Frame: Immediately post-intervention

Change in treatment-seeking intentions from baseline - higher score indicates higher help-seeking intentions (range of 3 to 12)

Self-Stigma Questionnaire - Post-Intervention

Time Frame: Immediately post-intervention

Change in stigma items from baseline - higher score indicates higher stigma (range of 15 to 60)

Help Seeking Intentions - Follow-Up

Time Frame: 30 days post-intervention

Change in treatment-seeking intentions from baseline - higher score indicates higher help-seeking intentions (range of 3 to 12)

Study Sites (1)

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