- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03710135
CDR Investing in Fatherhood Process Study & Evaluation
20. oktober 2018 opdateret af: 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.
Studieoversigt
Status
Ukendt
Betingelser
Detaljeret beskrivelse
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.
Undersøgelsestype
Observationel
Tilmelding (Forventet)
350
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Laura Parker, MPP
- Telefonnummer: 757-524-2271
- E-mail: lauraparkerconsulting@gmail.com
Studiesteder
-
-
Virginia
-
Williamsburg, Virginia, Forenede Stater, 23188
- Rekruttering
- Child Development Resources
-
Kontakt:
- Laura Parker
- Telefonnummer: 757-524-2271
- E-mail: lauraparkerconsulting@gmail.com
-
Ledende efterforsker:
- Laura Parker, MPP
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Parents (majority fathers) who participate in CDR's Pathways Fatherhood program, in the community and incarcerated individuals.
Beskrivelse
Inclusion Criteria:
- Any person enrolled in CDR's Pathways Fatherhood program.
Exclusion Criteria:
- Any participant who does not give informed consent.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in attitudes toward child
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. august 2016
Primær færdiggørelse (Forventet)
1. september 2020
Datoer for studieregistrering
Først indsendt
15. oktober 2018
Først indsendt, der opfyldte QC-kriterier
15. oktober 2018
Først opslået (Faktiske)
17. oktober 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
23. oktober 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
20. oktober 2018
Sidst verificeret
1. oktober 2018
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 2016/04/2
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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