- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00230009
Brief Intervention in At-Risk First-time Mothers
6. august 2013 opdateret af: Steven J. Ondersma, Wayne State University
Preliminary controlled trial of a brief intervention designed to reduce child maltreatment risk among low-income pregnant mothers.
Foci will include major risk factors for maltreatment, including substance abuse, social isolation, depression, violence exposure, and maladaptive child-rearing attitudes/beliefs.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
100
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Michigan
-
Detroit, Michigan, Forenede Stater, 48207
- Wayne State University
-
-
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
18 år til 45 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Pregnant, expecting first child
Inclusion Criteria:
Receipt of public assistance (e.g., Medicaid, Food Stamps), ability to communicate in English
Exclusion Criteria:
Frank psychosis or other cognitive impairment
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Ingen indgriben: Kun vurdering
|
|
Eksperimentel: Brief intervention session
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Alcohol Use
Tidsramme: 3 month follow-up
|
Alcohol use was measured by looking at frequency of use in past 30 days with the Alcohol Use Disorders Identification Test (AUDIT), reported at the 3 month follow-up.
The mean of each the control and intervention group was used.
Frequency of use ranged from 0 to 5 for the follow-up sample.
Higher scores mean more frequent use of the substance.
|
3 month follow-up
|
Drug Use
Tidsramme: 3 month follow-up
|
Drug use was measured by looking at frequency of use in past 30 days with the Alcohol Use Disorders Identification Test (AUDIT), reported about marijuana use at the 3 month follow-up.
The mean of each the assessment only and intervention group was used.
Scores ranged from 0 to 13 for the follow-up sample.
Higher scores mean more frequent use of the substance.
|
3 month follow-up
|
Child Abuse Potential
Tidsramme: baseline and 3 month follow-up
|
Change score was calculated by taking the follow-up scores on the Brief Child Abuse Potential Inventory (BCAP) and subtracting the baseline score.
The possible total score for the BCAP ranges from 0 to 24.
Therefore, the possible range of scores for the change calculation (reported below) is -24 to +24.
Higher scores indicate higher risk at the follow-up visit (worse outcome).
|
baseline and 3 month follow-up
|
Treatment Engagement
Tidsramme: at 3 month follow-up
|
The number of participants who reported seeking outpatient substance abuse treatment since baseline (either at a treatment facility or through outpatient counseling).
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at 3 month follow-up
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Depression
Tidsramme: at 3 month follow-up
|
Depression was measured by using the Center for Epidemiologic Studies Depression Scale (CES-D) at the 3 month follow-up.
CES-D total scores can range from 0 to 60. Scores at 16 or higher indicate clinical significance.
Higher scores represent higher risk for depression.
|
at 3 month follow-up
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Steven J Ondersma, Ph.D., Wayne State University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Delaney-Black V, Covington C, Ondersma SJ, Nordstrom-Klee B, Templin T, Ager J, Janisse J, Sokol RJ. Violence exposure, trauma, and IQ and/or reading deficits among urban children. Arch Pediatr Adolesc Med. 2002 Mar;156(3):280-5. doi: 10.1001/archpedi.156.3.280.
- Ondersma SJ, Chaffin MJ, Mullins SM, LeBreton JM. A brief form of the child abuse potential inventory: development and validation. J Clin Child Adolesc Psychol. 2005 Jun;34(2):301-11. doi: 10.1207/s15374424jccp3402_9. Erratum In: J Clin Child Adolesc Psychol. 2006 Dec;35(4):598.
- Mullins SM, Bard DE, Ondersma SJ. Comprehensive services for mothers of drug-exposed infants: relations between program participation and subsequent child protective services reports. Child Maltreat. 2005 Feb;10(1):72-81. doi: 10.1177/1077559504272101.
- Mullins SM, Suarez M, Ondersma SJ, Page MC. The impact of motivational interviewing on substance abuse treatment retention: a randomized control trial of women involved with child welfare. J Subst Abuse Treat. 2004 Jul;27(1):51-8. doi: 10.1016/j.jsat.2004.03.010.
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
1. april 2004
Primær færdiggørelse (Faktiske)
1. marts 2007
Studieafslutning (Faktiske)
1. marts 2007
Datoer for studieregistrering
Først indsendt
29. september 2005
Først indsendt, der opfyldte QC-kriterier
29. september 2005
Først opslået (Skøn)
30. september 2005
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
8. august 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
6. august 2013
Sidst verificeret
1. august 2013
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NIDA-00516-3
- K23DA000516 (U.S. NIH-bevilling/kontrakt)
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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