- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02371356
Comparing Effectiveness of Treating Depression With & Without Comorbidity to Improve Fetal Health (PCORIPTD)
12. marts 2020 opdateret af: Kaiser Permanente
Depression during pregnancy is prevalent (15-20%) and has an adverse impact on fetal outcomes including preterm delivery (PTD) and low birthweight (LBW).
Currently, significant confusion exists about if and how depression during pregnancy should be treated, given the unknown risk-benefit profiles of various treatments.
We propose to conduct a two-stage prospective cohort study to determine if treating depression in pregnancy is effective in improving fetal outcomes, and which treatment is most effective: pharmacotherapy, psychotherapy or a combination.
The risk-benefit of the treatments will be examined separately for two depression types: pregnant women with depression only and those with other psychiatric comorbidities to evaluate possible differences in treatment effectiveness between the two groups.
Findings will provide answers to long standing stakeholder questions of how to treat depression in pregnancy and which treatment is most effective with the best risk-benefit profile in improving fetal outcomes.
Selecting an effective treatment could reduce PTD or LBW, thus, reducing infant mortality and morbidity, and medical costs.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Depression during pregnancy is prevalent (15-20%) and has an adverse impact on fetal outcomes including preterm delivery (PTD) and low birthweight (LBW).
Currently, significant confusion exists about if and how depression during pregnancy should be treated, given the unknown risk-benefit profiles of various treatments.
Kaiser Permanente Northern California has implemented a large scale universal peripartum depression screening program, annually screening more than 35,000 pregnant women.
Taking advantage of this unique infrastructure, we propose to conduct a two-stage prospective cohort study to determine if treating depression in pregnancy is effective in improving fetal outcomes, and which treatment is most effective: pharmacotherapy, psychotherapy or a combination.
The risk-benefit of the treatments will be examined separately for two depression types: pregnant women with depression only and those with other psychiatric comorbidities to evaluate possible differences in treatment effectiveness between the two groups.
Stakeholders (patients, advocacy groups, and providers) are an integral part of the research team.
Four cohorts with different treatment options including untreated will be formed within each depression type (with or without comorbidity): (A) "Antidepressant only": screen positive for depression and use only antidepressants during pregnancy; (B) "Psychotherapy only": screen positive and receive psychotherapy only; (C) "Combination therapy": screen positive and receive both antidepressants and psychotherapy; (D)"Untreated depression": screen positive and receive no treatment.
A total of eight cohorts will be formed.
A final cohort (E) "No depression": screen negative and receive no treatment, will be examined for baseline comparison.
Information on depression treatment and PTD and LBW will be available for all participating women who will be followed until the end of pregnancy.
Within each depression category, comparison of Cohort A, B & C to D, respectively, will determine if treating depression is effective.
Pair-wise comparisons among Cohorts A, B & C will determine the comparative effectiveness of treatment regimens.
Comparison of Cohort D to E provides baseline fetal risks of untreated depression.
Findings will provide answers to long standing stakeholder questions of how to treat depression in pregnancy and which treatment is most effective with the best risk-benefit profile in improving fetal outcomes.
Selecting an effective treatment could reduce PTD or LBW, thus, reducing infant mortality and morbidity, and medical costs.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
91084
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 og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Kvinde
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Pregnant KPNC members who have been screened as part of KPNC's peripartum depression screening program, assigned to cohorts according to depression and treatment status.
Beskrivelse
Inclusion Criteria:
- Kaiser member
- Pregnant
Exclusion Criteria:
- Not a member of Kaiser Permanente
- Not pregnant
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
Depressed, Medication only
Screen positive for depression and use only antidepressants during pregnancy
|
|
Depressed, Psychotherapy only
Screen positive for depression and receive psychotherapy only.
|
|
Depressed, Medication & Psychotherapy
Screen positive for depression and receive both antidepressants and psychotherapy.
|
|
Depressed, untreated
Screen positive for depression and receive no treatment.
|
|
Not depressed
Screen negative for depression and receive no treatment.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Preterm Delivery
Tidsramme: Through the end of pregnancy, an average of 40 weeks
|
Delivery prior to 37 completed weeks of gestational age
|
Through the end of pregnancy, an average of 40 weeks
|
|
Low Birth Weight
Tidsramme: Through the end of pregnancy, an average of 40 weeks
|
Birth weight <2500 grams
|
Through the end of pregnancy, an average of 40 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
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 2014
Primær færdiggørelse (Faktiske)
31. januar 2017
Studieafslutning (Faktiske)
30. april 2019
Datoer for studieregistrering
Først indsendt
28. januar 2015
Først indsendt, der opfyldte QC-kriterier
24. februar 2015
Først opslået (Skøn)
25. februar 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
18. marts 2020
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. marts 2020
Sidst verificeret
1. marts 2020
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CN-13-1650-H
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
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