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NCT01482832 · ClinicalTrials.gov registry record · NA

Interpersonal Therapy-Based Treatment to Prevent Postpartum Depression in Adolescent Mothers

A NA study of Postpartum Depression, sponsored by Women and Infants Hospital of Rhode Island.

Completed
Registry status
NA
Development phase
250
Enrollment target
1
Study location

NCT01482832: Completed NA study of Postpartum Depression, sponsored by Women and Infants Hospital of Rhode Island.

NCT01482832 is a NA study of Postpartum Depression that has completed, run by Women and Infants Hospital of Rhode Island. The registered enrollment target is 250 participants, below the 470-participant average among 47 other Postpartum Depression trials with a reported enrollment target (47% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01482832, a NA study of Postpartum Depression, has completed, sponsored by Women and Infants Hospital of Rhode Island.

COMPLETED
Registry status
NA
Development phase
250 participants
Enrollment target
1
Study location

Study Summary

The Specific Aim of this study is to conduct a randomized controlled trial to evaluate whether Project REACH (an interpersonal psychotherapy-based intervention) compared with a didactic attention-control program reduces the risk of PPD in adolescent mothers. Primary Hypothesis: 1. The intervention (Project REACH) will be significantly more efficacious than the control program in reducing the risk of PPD up to six months postpartum in adolescent mothers. Secondary Hypotheses: 2. The decreased rate of major depression in the Project REACH group compared to the control program group will be sustained through one year postpartum. 3. Adolescent mothers in Project REACH compared to the control program group will have higher levels of maternal-child bonding.

Primary Outcome

Outcome assessment using KID-SCID

Conditions Studied

Interventions

  • BEHAVIORAL Interpersonal therapy-based treatment

Study Locations (1)

Rhode Island

  • Women & Infants Hospital - Providence

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2011-12
Est. Completion 2018-10-30
Phase NA

What the finished NCT01482832 record still lists

NCT01482832 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 470-participant average among 47 other Postpartum Depression trials with a reported enrollment target (47% lower).

The record links to 1 condition, with Postpartum Depression appearing as the primary indexed condition, and to 1 intervention - of which Interpersonal therapy-based treatment is the first listed.

NCT01482832 reports a single indexed study location in Rhode Island.

Frequently Asked Questions

What is clinical trial NCT01482832 about?

NCT01482832 is a clinical study titled "Interpersonal Therapy-Based Treatment to Prevent Postpartum Depression in Adolescent Mothers". The Specific Aim of this study is to conduct a randomized controlled trial to evaluate whether Project REACH (an interpersonal psychotherapy-based intervention) compared with a didactic attention-control program reduces the risk of PPD in adolescent mothers. Primary Hypothesis: 1. The intervention...

What is the current status of trial NCT01482832?

This trial is currently completed. It is a NA study. The enrollment target is 250 participants. The study started on 2011-12. Estimated completion is 2018-10-30.

What conditions does trial NCT01482832 study?

This clinical trial studies the following conditions: Postpartum Depression.

What interventions are being tested in trial NCT01482832?

The interventions under investigation include: Interpersonal therapy-based treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT01482832?

This trial is sponsored by Women and Infants Hospital of Rhode Island, which has 65 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01482832 being conducted?

This trial has 1 study location across Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Postpartum Depression

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01482832's enrollment target sits among peer trials

250 16th of 47 higher than 32 of 47 other Postpartum Depression trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Postpartum Depression trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01482832, the US trial registry maintained by the National Library of Medicine. NCT01482832 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.