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Minimum Intervention to Maintain a Postpartum Depression Prevention Program in Clinics Serving Low-income Women

A legfontosabb adatok

Ki végzi
Michigan State University
Hol
Flint (Egyesült Államok)A helyszín megnézése
Azonosító
Állapot
Befejeződött
Résztvevők
160 fő vett részt
Kezdés
2018. jún. 12.
Befejezés
2023. dec. 31.
A vizsgálat típusa
Beavatkozással járó, 3 csoport
A vizsgált kezelések
  • EIAU
  • LICF
  • HICF
A regiszteradat frissítve
2026. április 15.

Ki vehet részt

Életkor
18 év felett
Nem
Nők és férfiak
Egészséges önkéntesek
Nem vehetnek részt

A regiszter feltételei, szó szerint

Mind a 11 feltétel megnézéseKevesebb

Ki nem vehet részt

  • None

Egyéb feltételek

  • Study enrollment began with enrollment of clinics. Inclusion criteria for clinics were:
  • outpatient,
  • provide prenatal services,
  • estimate at least 30% of their pregnant patients received some kind of public assistance (such as federal or state cash assistance, food stamps, subsidized housing, and/or health insurance such as Medicaid),
  • have at least 3 new pregnant people per month on average (i.e., enough patient flow to run ROSE), and
  • agree to study procedures. Inclusion criteria were for the clinic itself; once the clinic was included, any pregnant person within the agency could receive ROSE; Participants were clinic personnel, and they were enrolled within clinic. Their inclusion criteria were:
  • age 18 or older
  • someone chosen by the agency to respond to quarterly survey questions about clinical delivery of ROSE (the "clinical respondent")
  • someone chosen by the agency to respond to quarterly surveys about operational (billing, scheduling) aspects of ROSE delivery (the "operational respondent," which could be the same or a different person than the "clinical respondent")
  • all ROSE facilitators for the agency (who completed self-rated ROSE adherence forms)

Helyszínek itt: Egyesült Államok

  • Michigan State UniversityFlint, Egyesült Államok

A vizsgálatról

Mit akar kideríteni a vizsgálat

Postpartum depression (PPD) is common and can have lasting consequences for mother and child. ROSE is an intervention to prevent PPD, delivered during pregnancy in outpatient prenatal settings. ROSE has been found to significantly reduce cases of PPD in multiple randomized trials in community prenatal settings with racially and ethnically diverse low-income pregnant women. Requests for ROSE training and recent policy changes supporting payment for comprehensive perinatal services to underserved populations suggest a context ripe for embedding ROSE in prenatal clinics long-term. Given the need for return on investment studies about sustainment efforts, we propose a Sequential Multiple Assignment Randomized (SMART) Trial of the effectiveness and cost-effectiveness of a stepwise approach to sustainment of ROSE in 90 outpatient clinics providing prenatal care to pregnant women on public assistance in 6 U.S. states. In Year 1, all clinics will receive enhanced implementation as usual (EIAU; initial training + tools for sustainment). At the first time at which a clinic is determined to be at risk for failure to sustain (i.e., at 3, 6, 9, 12, 15 months), that clinic will be randomized to receive either: (1) no additional implementation support (i.e., EIAU only), or (2) low-intensity coaching and feedback (LICF). If clinics receiving LICF are still found to be at risk at subsequent assessments, they will be randomized to either (1) EIAU + LICF only, or (2) high-intensity coaching and feedback (HICF). Additional study follow-up interviews will occur at 18, 24, and 30 months, but no implementation intervention will occur after 18 months. Outcomes include: 1. Sustainment of core program elements at each time point and total length of time ROSE services were provided and were provided with at least moderate fidelity. 2. Health impact (PPD rates over time at each clinic) and reach. 3. ROI (costs, cost-offsets, and cost-effectiveness) of each sustainment step. Hypothesized mechanisms include sustainment of clinical and organizational capacity to deliver core elements, and engagement/ownership. The study will also examine predictors, tailoring variables, and implementation processes to determine which kinds of clinics need which level of sustainment support and when. To our knowledge, this study will be the first randomized trial evaluating the ROI of a stepped approach to sustainment, a critical unanswered question in implementation science.

A vizsgálat 3 csoportja

  • Enhanced implementation as usual (EIAU)A vizsgált kezelés

    EIAU: Enhanced implementation as usual consists of initial training and problem-solving plus planning for sustainment.

    Kezelés: EIAU, LICF és HICF

  • Low-intensity coaching and feedback (LICF)A vizsgált kezelés

    Low-intensity (every 3 months) coaching and feedback (LICF): Enhanced implementation plus low intensity will have received initial training and problem-solving plus planning for sustainment and after that every 3 months will receive one clinical and one operational telephone "booster" meeting.

    Kezelés: LICF és HICF

  • High-intensity coaching and feedback (HICF)A vizsgált kezelés

    High-intensity (every month) coaching and feedback (HICF): Enhanced implementation plus high intensity will have received initial training and problem-solving plus planning for sustainment and after that every month will receive one clinical and one operational telephone "booster" meeting.

    Kezelés: HICF

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
Implementing to Sustain: Determining the Minimum Necessary Intervention to Maintain a Postpartum Depression Prevention Program (ROSE) in Clinics Providing Prenatal Services to Low-income Women
A regiszteradat frissítve
2026. április 15.