- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03710135
CDR Investing in Fatherhood Process Study & Evaluation
October 20, 2018 updated by: Laura Parker, Child Development Resources
Child Development Resources Investing in Fatherhood: New Pathways - Process Study & Evaluation
This study will evaluate the Investing in Fatherhood: New Pathways program of Child Development Resources (CDR), a Healthy Marriage and Responsible Fatherhood (HMRF) grantee.
The program will deliver parenting education, relationship skills training, job preparedness and financial planning, and case management support.
This research will consist of a descriptive process and program evaluation study, with research questions focusing on recruitment and retention and short-term participant outcomes.
Study Overview
Status
Unknown
Conditions
Detailed Description
This study will address three research questions:
- Which recruitment strategies are the most successful for participation? CDR will work to expand recruitment efforts and encourage greater participation through a number of strategies, such as offering various incentives and hosting classes in other spaces (e.g. churches, restaurants, clinics). This study will examine which methods are the most effective.
- Which engagement/retention strategies are the most successful? Current fatherhood services staff at CDR have expressed difficulty in getting fathers to participate on a regular and steady basis in fatherhood services. CDR will explore several strategies for increased retention and this study will evaluate these strategies.
- Do fathers who participate in the program earlier in their fatherhood experience (e.g. when their oldest child is under five years of age) report better outcomes than fathers who begin receiving fatherhood services later? CDR has extensive knowledge working specifically with young children and families in early intervention programs. In early childhood development, many studies have shown that the highest return on investment comes from early intervention, from birth through age five. The hypothesis is that this principle holds true in responsible fatherhood programming as well.
Study Type
Observational
Enrollment (Anticipated)
350
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Virginia
-
Williamsburg, Virginia, United States, 23188
- Recruiting
- Child Development Resources
-
Contact:
- Laura Parker
- Phone Number: 757-524-2271
- Email: lauraparkerconsulting@gmail.com
-
Principal Investigator:
- Laura Parker, MPP
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Parents (majority fathers) who participate in CDR's Pathways Fatherhood program, in the community and incarcerated individuals.
Description
Inclusion Criteria:
- Any person enrolled in CDR's Pathways Fatherhood program.
Exclusion Criteria:
- Any participant who does not give informed consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in attitudes toward child
Time Frame: depending on program length, ranges from 30 days to 10 weeks
|
nFORM (Information, Family Outcomes, Reporting, and Management) questions on pre- and post-survey.
Answers range from (1) Never to (4) Often.
A higher response indicates a better outcome.
|
depending on program length, ranges from 30 days to 10 weeks
|
|
Change in using negative punishment with child
Time Frame: depending on program length, ranges from 30 days to 10 weeks
|
nFORM (Information, Family Outcomes, Reporting, and Management) questions on pre- and post-survey.
Answers range from (1) Never to (4) Every Day or Almost Every Day.
A lower response indicates a better outcome.
|
depending on program length, ranges from 30 days to 10 weeks
|
|
Change in time spent with child
Time Frame: depending on program length, ranges from 30 days to 10 weeks
|
nFORM (Information, Family Outcomes, Reporting, and Management) questions on pre- and post-survey.
Answers range from (1) Never to (4) Every Day or Almost Every Day.
A higher response indicates a better outcome.
|
depending on program length, ranges from 30 days to 10 weeks
|
|
Change in feeling overwhelmed with parenting responsibilities
Time Frame: depending on program length, ranges from 30 days to 10 weeks
|
nFORM (Information, Family Outcomes, Reporting, and Management) questions on pre- and post-survey.
Answers range from (1) Never to (4) Often.
A lower response indicates a better outcome.
|
depending on program length, ranges from 30 days to 10 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2016
Primary Completion (Anticipated)
September 1, 2020
Study Registration Dates
First Submitted
October 15, 2018
First Submitted That Met QC Criteria
October 15, 2018
First Posted (Actual)
October 17, 2018
Study Record Updates
Last Update Posted (Actual)
October 23, 2018
Last Update Submitted That Met QC Criteria
October 20, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 2016/04/2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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