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Treatment Education for Perinatal Women and Their Community Support

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Johns Hopkins University

Status

Begins enrollment in 4 months

Conditions

Opioid Dependency

Treatments

Other: substance abuse treatment education

Study type

Interventional

Funder types

Other

Identifiers

NCT06733649
IRB00478467

Details and patient eligibility

About

The study evaluates the feasibility and acceptability of a 50 minute treatment education session for perinatal women with opioid use disorder and a community support person. The education session provides correct information about opioid agonist medications and neonatal abstinence syndrome.

Full description

Perinatal women with opioid disorder often face criticism by social network members for receiving opioid agonist treatment. Feeling stigmatized by others may impact willingness to start and remain in agonist treatment.

The present study evaluates the feasibility and acceptability of a 50 minute treatment education session for perinatal women who are treated using an agonist medication (methadone or buprenorphine) and community support chosen by the patient.

Study participants will be recruited from perinatal women who receive substance abuse treatment at the Center for Addiction and Pregnancy or Addiction Treatment Services at Johns Hopkins Bayview campus. These women will work with a counselor to select a community support person to bring to the program for the education session.

The session will provide correct information on opioid agonist medications and neonatal abstinence syndrome. This session will follow a structured outline.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • perinatal women treated with agonist medication
  • interest in study participation
  • interest in community support:
  • interest in study participation

Exclusion criteria

  • perinatal women not treated with agonist medication
  • not interested in study participation
  • not interested in community support:
  • not interested in study participation

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

Treatment education for perinatal women and the womens' community support
Experimental group
Treatment:
Other: substance abuse treatment education

Trial contacts and locations

0

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Central trial contact

Denis Antoine, MD; Michael Kidorf, Ph.D.

Data sourced from clinicaltrials.gov

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