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Clinical Trials/NCT03921892
NCT03921892
Completed
Not Applicable

A Randomized Feasibility and Acceptability Study Comparing In-person to On-line Parenting Education for Adolescent Fathers

University of Missouri, Kansas City3 sites in 1 country10 target enrollmentSeptember 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adolescent, Parenting
Sponsor
University of Missouri, Kansas City
Enrollment
10
Locations
3
Primary Endpoint
Feasibility Measure 1
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This feasibility and acceptability study will compare in-person to web-based parenting education for adolescent fathers on the outcomes of parenting confidence and participation in parenting activities.

Detailed Description

This is a randomized feasibility and acceptability study using a block generator for randomization of participants aged 15 to 21 into either in-person parenting education or on-line parenting. Outcome measures include parenting self-efficacy and participation in daily parenting activities. Participants will take part in approximately twelve hours of parenting education, whether in-person or on-line. Recruitment flyers will be placed in two primary care clinics and a large regional hospital's Labor \& Delivery and Postpartum (Mother-Baby) Units. Participants will seek out the opportunity to participate by calling the phone number or sending an e-mail to the investigators to learn more about the study and their potential participation. If participants meet eligibility criteria and elect to participate, baseline measurements will be completed after enrollment, with follow-up measures at one month and two months.

Registry
clinicaltrials.gov
Start Date
September 15, 2019
End Date
September 15, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rita Sue Lasiter

Principal Investigator

University of Missouri, Kansas City

Eligibility Criteria

Inclusion Criteria

  • age 15 to 21,
  • be able to read and understand English (as determined by having the individual read a brief, eighth grade reading level paragraph),
  • able to begin the intervention within six weeks of their infant's birth,
  • be able to participate in an intervention over two weeks, requiring approximately a 12-hour time commitment: either in-person on two Saturdays for six hours each, or a self-paced content of videos and resource materials over two weeks,
  • own or have access to a device with internet access and
  • have a working e-mail address.

Exclusion Criteria

  • Any condition that might prevent the father's infant from reaching normal developmental milestones will participation, including congenital malformations or prematurity requiring prolonged/ ongoing infant hospitalization.

Outcomes

Primary Outcomes

Feasibility Measure 1

Time Frame: 12 months

Did recruitment numbers meet goals

Feasibility Measure 2

Time Frame: 12 months

Attrition rate of participants

Acceptability Survey Measure 1 (Likert Scale)

Time Frame: 12 months

Acceptability of learning content to participants

Acceptability Survey Measure 2 (Likert Scale)

Time Frame: 12 months

Acceptability of time burden to participants

Feasibility Measure 3

Time Frame: 12 months

Percent of data missing from data collection tools

Acceptability Survey Measure 3 (Likert Scale)

Time Frame: 12 months

Acceptability of learning method to participants

Secondary Outcomes

  • What is the difference between in-person education as compared to on-line parenting education on parental self-efficacy of adolescent fathers as measured by the Parenting Sense of Competence Scale (PSOC)?(12 months)
  • What is the difference between in-person parenting education as compared to on-line parenting education on participation in parenting activities of adolescent fathers as measured by the Child Care Activities Scale (CCAS)?(12 months)

Study Sites (3)

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