- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02444325
Diabetes Group Prenatal Care
3. januar 2018 opdateret af: Washington University School of Medicine
Group Prenatal Care for Women With Diabetes: A Pilot Randomized Control Trial
The investigators primary objective is to conduct a pilot randomized trial to determine the effect of group prenatal care on self-care activities in women with diabetes.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Long term, the investigators aim to test the central hypothesis that group prenatal care, compared to traditional prenatal care, will improve glycemic control and, ultimately, maternal and neonatal outcomes in women with type 2 and gestational diabetes.
The objective of this proposal is to conduct a pilot randomized trial to determine the effect of group prenatal care on self-care activities, which have been associated with improved glycemic control, in women with diabetes.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
84
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Colorado
-
Denver, Colorado, Forenede Stater, 80204
- Denver Health
-
-
Missouri
-
Saint Louis, Missouri, Forenede Stater, 63110
- Washington University in St. Louis
-
-
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 50 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- English (WUMC) or Spanish speaking (DH)
- Type 2 White's Class B diabetes OR gestational diabetes diagnosed by 2-step method < 32 weeks
- Ability to attend group prenatal visit at specified days and times
- Willingness to be randomized
- Randomization at 22 weeks 0 days-32 weeks 0 days
- Ability to give informed consent
Exclusion Criteria:
- Multiple gestation
- Major fetal anomaly
- Serious medical co-morbidity necessitating more care than can be safely provided in group setting, as deemed by medical provider
- Serious psychiatric illness including schizophrenia necessitating more care than can safely be provided in group setting, as deemed by medical provider
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Ingen indgriben: Routine Prenatal Care
Subjects randomized to routine care will receive their care in the usual diabetic clinic attended by residents and faculty.
They will receive consultation with the diabetes educator at diagnosis and as needed.
Patients are seen every 2 weeks (or more by provider discretion) until 37 weeks and weekly until delivery.
Visits are 10-15 minutes and focus on routine screening tests and review of blood sugar logs/medication titration.
Each subject's medical chart will be reviewed for demographics, antenatal management, maternal and neonatal outcomes.
|
|
Eksperimentel: Group prenatal care
Group visits will be held every 2 weeks in a continuous cycle through a four session curriculum.
Women will have weekly visits beginning at 37 weeks with traditional prenatal visits on the weeks when the group does not meet.
Groups of 4-12 women will meet for two hour visits and much of that time will be spent on pregnancy, behavioral health, diabetes and nutrition education.
Groups will be co-facilitated by 2 CenteringPregnancy trained providers at each site and an obstetric provider.
Women may be instructed to have additional visits in the traditional clinic at the discretion of the obstetric provider.
|
Women will receive their prenatal care in a group rather than in the 1:1 traditional manner.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
effect of group prenatal care on maternal diabetes self-care activities as measured Diabetes Self-Care Activities Measure
Tidsramme: 37-39 weeks gestation
|
Determine the effect of group prenatal care on maternal diabetes self-care activities as measured by the Diabetes Self-care Activities Measure and confirmed by percentage of recommended blood glucose values completed on logs since initial study visit.
|
37-39 weeks gestation
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
effect of group prenatal care on perinatal mood as measured by Edinburgh Postnatal Depression Scale
Tidsramme: baseline and 4-12 weeks postpartum
|
Determine the effect of group prenatal care on perinatal mood as measured by the Edinburgh Postnatal Depression Scale
|
baseline and 4-12 weeks postpartum
|
effect of group prenatal care on perceived social support as assessed by the Social Support Scale
Tidsramme: 37-39 weeks
|
Determine the effect of group prenatal care on perceived social support through the Social Support Scale
|
37-39 weeks
|
Birthweight
Tidsramme: delivery admission
|
Determine the effect of group prenatal care on birthweight
|
delivery admission
|
Gestational age at delivery
Tidsramme: delivery admission
|
Determine the effect of group prenatal care on preterm delivery
|
delivery admission
|
Mean 3rd trimester fasting blood glucose
Tidsramme: baseline through delivery
|
Determine the effect of group prenatal care on maternal glycemic control through mean 3rd trimester fasting glucose
|
baseline through delivery
|
Breastfeeding
Tidsramme: 4-12 weeks postpartum
|
Determine the effect of group prenatal care on initiating breastfeeding
|
4-12 weeks postpartum
|
Contraception
Tidsramme: 4-12 weeks postpartum
|
Determine the effect of group prenatal care on initiating contraception
|
4-12 weeks postpartum
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Studieleder: Methodius G Tuuli, MD, MPH, Assistant Professor, Washington University in St. Louis
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. maj 2015
Primær færdiggørelse (Faktiske)
6. juli 2017
Studieafslutning (Faktiske)
27. september 2017
Datoer for studieregistrering
Først indsendt
27. april 2015
Først indsendt, der opfyldte QC-kriterier
13. maj 2015
Først opslået (Skøn)
14. maj 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
5. januar 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. januar 2018
Sidst verificeret
1. januar 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 201503174
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 .
Kliniske forsøg med Graviditet
-
King's College Hospital NHS TrustEuropean Association for the Study of the LiverRekrutteringCirrhose, lever | HELLP syndrom | Intrahepatisk kolestase af graviditet | Graviditetssygdom | AFLP - Acute Fatty Lever of PregnancyDet Forenede Kongerige
Kliniske forsøg med Group prenatal care
-
Yale UniversityBrown UniversityAfsluttet
-
San Diego State UniversityRekrutteringDepression | Stress | Graviditetsrelateret | Forskelsbehandling, racemæssig | Psykisk sundhedsproblemForenede Stater
-
Centro de Atenção ao Assoalho PélvicoIndústria Brasileira Equipamentos Médicos - IBRAMEDRekrutteringErektil dysfunktionBrasilien
-
RenJi HospitalIkke rekrutterer endnuFlydende reaktionsevne | Slagvolumen variation | SVV-FloTrac | Thorax elektrisk bioimpedansKina
-
RenJi HospitalIkke rekrutterer endnuFlydende reaktionsevne | Slagvolumen variation | SVV-FloTrac | Thorax elektrisk bioimpedansKina
-
Ayşegül İşler DalgıçHorizonIkke rekrutterer endnuStress, følelsesmæssig | Sundhedsrisikoadfærd | Sundhedsrelateret adfærd | Sund livsstil | Fysisk inaktivitet | Sund ernæring | Indeks for sund kost | Ikke-smitsomme sygdommeKalkun
-
Boston Medical CenterNational Institute of Mental Health (NIMH)AfsluttetPost traumatisk stress syndromForenede Stater
-
Hui-Hsun ChiangAfsluttetUddannelsesmæssige problemer | Ammende | Vold på arbejdspladsenTaiwan
-
University of California, San FranciscoMount Zion Health Fund; Pritzker Family Foundation; Mental Insight FoundationAfsluttetDepression, UnipolarForenede Stater