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Clinical Trials/NCT06969248
NCT06969248Active, not recruitingNot Applicable

The Effects of Interventions Targeted to Fathers on Fathers' Participation in Infant Care, Attachment Status, and Paternal Depression: A Randomized Controlled Trial

Selcuk University1 site in 1 country80 target enrollmentStarted: January 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
80
Locations
1
Primary Endpoint
Fathers' Involvement in Infant Care Questionnaire

Study Overview

Brief Summary

Fathers participating in the study will be given an 8-week formality intervention. Participants will be shown 4-week infant care training records and then 4-week videos prepared on educational topics. The effect of the intervention will be determined annually by the mean scores of the Fathers' Participation in Infant Care Questionnaire, Father Infant Attachment Scale, and Edinburgh Postpartum Depression Scale.

Detailed Description

The study will be conducted in a Family Health Center in Turkey, selected by random lottery. Fathers who are registered in a family health center and have babies aged 4-12 months and fathers who have children for the first time will be included in the study. The type of the study is planned as randomized controlled pre-test post-test, parallel group experimental type. A total of 80 fathers will be included in the study, 40 in each group, according to the calculation made with Gpower analysis. Participants will be randomly assigned to groups. Nursing interventions will last for 8 weeks and participants will be given training and watched videos during this process.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Masking Description

Since the trainings for the experimental group in the study will be conducted by the researcher conducting the study, researcher and participant blinding will not be possible. The data will be analyzed by an independent statistics expert. In this context, statistical blinding will be applied.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Having a healthy baby between 4-12 months old,
  • •Being a first-time father,
  • •Volunteering to participate in the study,
  • •Having a smartphone

Exclusion Criteria

  • •Being under 18 years old,
  • •Having a psychiatric diagnosis.

Arms & Interventions

Non-Intervention Group

No Intervention

Fathers in the control group will continue their routine practices. Fathers in this group will be measured twice, pre-test and post-test. No intervention will be made to the control group. After the intervention group's training is completed, training contents and videos will be shared with the control group.

Intervention Group

Experimental

Intervention: Intervention Group (Behavioral)

Outcomes

Primary Outcomes

Fathers' Involvement in Infant Care Questionnaire

Time Frame: 8 week

Father Infant Attachment Scale

Time Frame: 8 week

Edinburgh Postpartum Depression Scale

Time Frame: 8 week

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tuba Demirel

Assoc.Prof.

Selcuk University

Study Sites (1)

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