- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05337215
The Effect of Postpartum Kangaroo Father Care on Paternal Attachment (kangaroocare)
The Effect of Postpartum Kangaroo Father Care on Paternal Attachment: A Randomized Controlled Study Turkey Sample
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective: This study was conducted in a randomized controlled manner to determine the effect of kangaroo care (KC) on paternal attachment (PA).
Design: The data for the study were collected using the introductory information form (IIF) and the father-infant attachment scale (FIAS). T test, Mann Whitney U test and Kruskal Wallis test were used for statistical analysis.
Participants and setting: A total of 90 fathers, including 45 in the intervention group and 45 in the control group who met the inclusion criteria of the study were included randomly.
Keywords: Kangaroo care; father; paternal attachment; Turkey.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Çorum
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Corum, Çorum, Turkey, 19600
- Fatma Yıldırım
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- fathers who are aged 18 and 50,
- married,
- voluntarily agree to participate in the study,
- have healthy babies,
- live with their babies.
Exclusion Criteria:
- a history of chronic psychiatric illness
- antipsychotic medication use
- babies with premature / low birth weight / congenital anomalies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control group
While the IIF was applied to control group at the first meeting in the postpartum ward, FIAS was administered by phone or home visit in the third month after the face-to-face interview.There was any intervention for this group
|
The effect of postpartum kangaroo father care on paternal attachment
|
|
Experimental: kangaroo father care
While the IIF was applied to control group at the first meeting in the postpartum ward, FIAS was administered by phone or home visit in the third month after the face-to-face interview.. the first KC was applied within the first 4-6 hours after birth, and the second KC was applied in the postpartum ward under the supervision of the researcher on the first day after birth.
The third KC was performed by the fathers themselves at home on the third postpartum day after discharge.
Immediately afterwards, the researcher observed the father and baby from an appropriate distance, and the father and the baby had skin-to-skin contact for mean 15-20 minutes.
|
The effect of postpartum kangaroo father care on paternal attachment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Father-Baby Attachment Scale The Turkish version
Time Frame: 12 months
|
Father-Baby Attachment Scale The Turkish version was applied by Güleç and Kavlak (2013) to the fathers of infants aged 6-12 months, and the McDonald coefficient was reported to be between 0.52 and 0.80 (Güleç and Kavlak 2013).
The scale consists of 19 items and three sub-dimensions: "patience and tolerance".
"pleasure in interaction", and "love and pride".
Each item on the scale is scored between 1 and 5 points.
The minimum score that can be obtained from the scale is 19 and the maximum is 95.
High scores indicate that the attachment level is high.
|
12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HititUniversity_2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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