Family Spirit Study
Completed · Not applicable
Conditions studied: Substance Abuse
In brief
The goals of this study are to evaluate the effects of an in-home parenting education program, called Family Spirit, on parenting knowledge and skills and decreasing alcohol and substance use compared to a breast-feeding education. In addition, we will assess aspects of mother/child interaction.
Key facts
- Study ID
- NCT00356551
- Run by
- Johns Hopkins University
- People needed
- 320
- Starts
- 2002-05-01
- Expected to finish
- 2005-09-01
- Last updated by the study team
- 2016-08-01
Who can join
Age: 12 and older, up to 24. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Native American pregnant teens or young women ages 12-22 years old at the time of conception.
- Women ages 20-22 years at the time of conception must be pregnant for the first time.
- Partners of pregnant teens must be between the ages of 12-24.
- Pregnant <28 weeks gestation and able to meet the requirements for completing the program in a timely way.
- An enrolled tribal member.
- Reside in the Reservation Service Unit Catchment Area and within 60 mile of the Indian Health Service Unit Headquarters.
You may not qualify if…
- Severe mental illness - schizophrenia, bipolar disorder, incapacitating depression, or Substance abuse/dependence in need of intensive and specific treatment
- Active legal problems - subjects will not be enrolled if they are incarcerated or if program participation has been made a condition of parole
- Ongoing social service involvement for abuse and neglect
Where it is running
- Johns Hopkins Center for American Indian Health — Fort Defiance, Arizona, United States
- Johns Hopkins Center for American Indian Health — Tuba City, Arizona, United States
- Johns Hopkins Center for American Indian Health — Whiteriver, Arizona, United States
- Johns Hopkins Center for American Indian Health — Baltimore, Maryland, United States
- Johns Hopkins Center for American Indian Health — Gallup, New Mexico, United States
Full record on ClinicalTrials.gov
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