NCT05915416

Brief Summary

The aim of this study is to determine the effect of the Child Abuse and Neglect Prevention Program (CANPP) based on Social Cognitive Theory (SCT) on the awareness levels and child abuse potential of pregnant women. This randomized controlled study was conducted between July and December 2022 in a family health center of Aydin/Turkey with the participation a total of 30 pregnant women, who were then distributed into two groups as 15 experiment group and 15 control group pregnant women.The participants in the experiment group were applied SCT-based CANPP whereas no intervention was applied to the control group. Research data were collected before the intervention, one month after the intervention, and three months after the intervention using the Pregnant Data Collection Form, Child Neglect and Abuse Awareness Scale for Parents (CNAASP) and Child Abuse Potential Inventory (CAPI). Chi-Square and Fisher exact tests, independent groups t-test and repeated measures ANOVA test were used in the statistical analysis of the research data.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2022

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2022

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 13, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 23, 2023

Completed
Last Updated

June 23, 2023

Status Verified

June 1, 2023

Enrollment Period

1 month

First QC Date

June 13, 2023

Last Update Submit

June 21, 2023

Conditions

Keywords

child abuseawarenesspregnantnurse

Outcome Measures

Primary Outcomes (2)

  • Child Neglect and Abuse Awareness Scale for Parents

    Child Neglect and Abuse Awareness Scale for Parents is a 5-point Likert-type scale (1-strongly disagree, 2-disagree, 3-undecided, 4-agree, 5-strongly agree) and consisting of 45 items in total. The scale has 5 sub-dimensions namely General Information (12 items), Physical Abuse (6 items), Emotional Abuse (15 items), Sexual Abuse (8 items), Neglect (4 items). By adding all sub-dimensions, the Child Neglect and Abuse Awareness Scale for Parents total score is calculated. The higher this total score, the higher the awareness of child abuse and neglect.

    one month after the intervention

  • Child Neglect and Abuse Awareness Scale for Parents

    Child Neglect and Abuse Awareness Scale for Parents is a 5-point Likert-type scale (1-strongly disagree, 2-disagree, 3-undecided, 4-agree, 5-strongly agree) and consisting of 45 items in total. The scale has 5 sub-dimensions namely General Information (12 items), Physical Abuse (6 items), Emotional Abuse (15 items), Sexual Abuse (8 items), Neglect (4 items). By adding all sub-dimensions, the Child Neglect and Abuse Awareness Scale for Parents total score is calculated. The higher this total score, the higher the awareness of child abuse and neglect.

    three months after the intervention

Secondary Outcomes (2)

  • Child Abuse Potential Inventory

    one month after the intervention

  • Child Abuse Potential Inventory

    three month after the intervention

Study Arms (2)

Experiment Group

EXPERIMENTAL

The participants in the experiment group were first administered the pre-test and then CANPP. A Child abuse and neglect Training Booklet was sent to the participants after the pre-test and before the program. Trainings within the scope of CANPP were provided over the Google Meet application in four sessions. A link was sent to the pregnant women via WhatsApp just before the specified training hours so that they could participate in the online training which is carried out individually.

Behavioral: Child Abuse and Neglect Prevention Program

Control group

NO INTERVENTION

Participants in control group does not receive intervention. They were then applied CANPP and were given the training booklet after the finalization the program.

Interventions

The Child Abuse and Neglect Prevention Program was then revised in line with the opinions and suggestions of the experts. Power-point presentations and training booklet prepared for the final form of this program have been prepared in such a way that the content is exactly the same. Training booklet was distributed to the experiment group after the pre-test and to the control group after the re-test. This booklet is designed as a resource that participants can refer to whenever they need it. Trainings were provided online through the Google Meet application, in a total of four sessions with an average of 30 minutes per session. The contents of the trainings are child neglect, physical abuse, emotional abuse and sexual abuse, respectively. Four different power-point presentations, addressing these sub-dimensions, were prepared for training purposes.

Experiment Group

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Pregnant women who agree to participate in the study
  • are 18 years of age or older
  • who can read and understand Turkish
  • who have either a smart phone or a computer
  • are between 28+0 and 33+0 weeks of pregnancy

You may not qualify if:

  • Pregnant women with high risk pregnancy
  • who have visual or auditory problems
  • who have been diagnosed with mental disorders.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Koç University

Istanbul, 34100, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Researcher and participants could not be blinded due to the nature of the research. Data were coded as 'A' for experiment group and 'B' for control group. Statistical analysis of the coded data was performed by a statistics professional in order to avoid bias in the statistical evaluation of research data.
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator, Dr

Study Record Dates

First Submitted

June 13, 2023

First Posted

June 23, 2023

Study Start

July 1, 2022

Primary Completion

August 1, 2022

Study Completion

December 1, 2022

Last Updated

June 23, 2023

Record last verified: 2023-06

Data Sharing

IPD Sharing
Will not share

Locations