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Completed

NCT Number: NCT01177982

Reinforcement-Based Treatment for Pregnant Drug Abusers

Objectives: This project is a Stage II behavioral development study designed to answer remaining critical questions necessary before disseminating Reinforcement Based Treatment (RBT) to the larger treatment community. These questions focus on the levels of intensity of RBT most efficacious for substance-using pregnant patients. Design: The proposed study utilizes a novel approach to conducting a controlled clinical trial, the sequential multiple assignment randomized trial (SMART) design. Participants (N=220) will first be randomized at treatment outset into either treatment-as-usual RBT or a reduced intensity RBT. All participants will receive a subsequent randomization based upon an assessment of their initial two weeks of treatment compliance. Early-non-compliant participants will be randomized to receive either the same or an increased level of RBT treatment intensity while early-compliant participants will be randomized to receive either the same or decreased level of treatment intensity and scope. Primary outcome measures include treatment completion, and maternal heroin, cocaine, and other illicit substance use. Secondary outcome measures include maternal measures of HIV risk behavior, and psychosocial functioning and neonatal measures of length of hospitalization, and birth outcomes. Significance: The proposed project's innovation includes: the novelty RBT, use of a cutting-edge SMART model, application of advanced statistical techniques and inclusion of a cost-effectiveness approach. The proposed project's significance is exceedingly high, as it will lay the foundation for later Stage III studies focused on dissemination of stepped care treatment programs for drug-addicted pregnant women that can be implemented not only in comprehensive care clinics but in diverse community settings that provide services to such women.

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Key information

Age range

18 year–46 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Johns Hopkins Bayview Medical Center

Baltimore, Maryland, 21224, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Treatment entry at or before 34 weeks EGA with singleton fetus.
  • Evidence of opioid, cocaine and/or other primary illicit substance use.

Exclusion criteria

  • Severe medical or psychiatric concomitant condition interfering with treatment or needing hospitalization.
  • Age 17 years or younger.
  • Geographical constraints. These women are admitted only for a residential detoxification and often have plans to obtain aftercare in an outpatient or residential facility in closer proximity to their home. Thus, this greater distance from CAP increases the likelihood that these women will not return to CAP and will not deliver in a hospital that functions under similar protocols that operate in Baltimore City for treating drug-exposed neonates.

Treatment and study plan

Usual RBT (t-RBT)

Behavioral

Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach Social Club Job Club

Reduced RBT (r-RBT)

Behavioral

Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach

Abbreviated RBT (a-RBT)

Behavioral

Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Recreation

Enhanced RBT (e-RBT)

Behavioral

Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach Social club Job Club Recovery housing CAP housing admission Recovery sponsor

Early compliant t-RBT

Behavioral

r-RBT Individual therapy Skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach t-RBT: Social club Job club

Early non-compliant t-RBT

Behavioral

t-RBT Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach Social club Job club e-RBT: Recovery housing CAP short term housing admission Recovery sponsor

Early compliant r-RBT

Behavioral

a-RBT Individual therapy CBT skills modules Functional assessment Behavior contracts Behavior graphing Recreation r-RBT: Individual therapy Skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach

Early non-compliant r-RBT

Behavioral

r-RBT Individual therapy Skills modules Functional assessment Behavior contracts Behavior graphing Tangible rewards MI feedback Recreation Outreach t-RBT: Social Club Job Club

Primary outcomes

  1. Treatment Completion

    Time frame: Delivery (data extracted from medical record)

    Delivering a baby, regardless of delivery hospital, while enrolled in treatment.

  2. Substance use

    Time frame: Once monthly until delivery and at six weeks post-partum

    Drug Use: Urinalysis testing and self reported use (days in past month) for opioids, cocaine and other illicit substance use.

Secondary outcomes

  1. Alcohol

    Time frame: Once monthly until delivery and at six weeks post-partum

    Alcohol use: Urinalysis testing and self-reported (days in past month) of alcohol use

  2. Maternal Obstetrical Course/Outcome

    Time frame: Delivery (data extracted from medical record)

    Available maternal data will be abstracted from the completed delivery record (i.e.., maternal urine toxicology results at delivery, complications during labor/delivery, placental abruption, type of delivery, maternal length of hospital stay).

  3. Birth outcomes

    Time frame: Delivery (data extracted from medical record)

    Available birth outcome data will be extracted from infant medical records (i.e., birth weight, gestational age, infant complications).

  4. Length of Hospital Stay

    Time frame: Upon release of infant from hospital (data extracted from medical record)

    Length of hospital stay is an indicator of health and well-being. The total days in the Newborn Nursery, Pediatrics and Neonatal Intensive Care will be abstracted from the medical records.

  5. APGAR scores

    Time frame: Delivery (data extracted from medical record)

    Scores assigned at 1 and 5 minutes and any additional Apgar scoring if applicable will be extracted from the infant medical record

Sponsors and collaborators

Lead sponsor

National Institute on Drug Abuse (NIDA)

Nih

Collaborators

  • Johns Hopkins University

Registry information

Acronym: HOME II

Important dates

Study start
2009
Primary completion
2014
Study completion
2015
First posted
Aug 9, 2010
Registry last updated
Jan 11, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.