Integrating Interventions for Maternal Substance Abuse

NCT ID: NCT01188434

Last Updated: 2015-04-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-09-30

Study Completion Date

2012-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This Research Plan proposes Stage 1 Research integrating evidence based practices to address the needs of mothers referred to child welfare for substance abuse. Mothers with a history of methamphetamine abuse and child neglect will be recruited. Using an intensive community based treatment, mothers will receive substance abuse treatment combined with parenting skills training and psychosocial support for basic needs (e.g., housing, employment). This project will include a feasibility study (n = 5), followed by a small randomized pilot (n = 24) to examine the efficacy of the Integrated Treatment for Substance Abuse and Neglect compared to treatment as usual, with a population of substance abusing neglectful mothers referred through the Department of Child Welfare.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Substance Abuse Child Neglect

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Integrated Behavioral Treatment

Combined substance abuse, parenting skills, and basic needs intervention

Group Type EXPERIMENTAL

ITSAN

Intervention Type BEHAVIORAL

integrated behavioral intervention for substance abuse, parenting skills, and basic needs

casework treatment as usual

services as usual as referred by child welfare

Group Type ACTIVE_COMPARATOR

Services as Usual

Intervention Type BEHAVIORAL

Services as usual referred by child welfare

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

ITSAN

integrated behavioral intervention for substance abuse, parenting skills, and basic needs

Intervention Type BEHAVIORAL

Services as Usual

Services as usual referred by child welfare

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Maternal Substance Abuse
* Child Welfare involvement
* Child Neglect
* English Speaking
* Child either remaining in the home or reunification plan in place
* Living in the county

Exclusion Criteria

* Current involvement in other substance abuse treatment
* Current involvement in other parenting skills training
* parental rights terminated
* active psychosis
Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Oregon Social Learning Center

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Lisa Saldana

Research Scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Lisa Saldana, PhD

Role: PRINCIPAL_INVESTIGATOR

OSLC Community Programs

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

OSLC

Eugene, Oregon, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

K23DA021603

Identifier Type: NIH

Identifier Source: org_study_id

View Link

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.