CDR Investing in Fatherhood Process Study & Evaluation
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03710135 |
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Recruitment Status : Unknown
Verified October 2018 by Laura Parker, Child Development Resources.
Recruitment status was: Recruiting
First Posted : October 17, 2018
Last Update Posted : October 23, 2018
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| Condition or disease |
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| Parenting Parent-Child Relations |
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 |
| Estimated Enrollment : | 350 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Prospective |
| Official Title: | Child Development Resources Investing in Fatherhood: New Pathways - Process Study & Evaluation |
| Actual Study Start Date : | August 1, 2016 |
| Estimated Primary Completion Date : | September 2020 |
- 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.
- 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.
- 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.
- 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.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Any person enrolled in CDR's Pathways Fatherhood program.
Exclusion Criteria:
- Any participant who does not give informed consent.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03710135
| Contact: Laura Parker, MPP | 757-524-2271 | lauraparkerconsulting@gmail.com |
| United States, Virginia | |
| Child Development Resources | Recruiting |
| Williamsburg, Virginia, United States, 23188 | |
| Contact: Laura Parker 757-524-2271 lauraparkerconsulting@gmail.com | |
| Principal Investigator: Laura Parker, MPP | |
| Responsible Party: | Laura Parker, Local Evaluator, Child Development Resources |
| ClinicalTrials.gov Identifier: | NCT03710135 |
| Other Study ID Numbers: |
2016/04/2 |
| First Posted: | October 17, 2018 Key Record Dates |
| Last Update Posted: | October 23, 2018 |
| Last Verified: | October 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

