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Beginning Relationships in a Native Community (P20-RP3)

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University of Washington

Status

Completed

Conditions

Parent-child Interaction

Treatments

Behavioral: Immediate Group
Behavioral: Wait-List group

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02091804
STUDY00001796
1P20MD006871 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to to conduct a randomized controlled trial comparing an intervention group and a control/wait list group to evaluate the feasibility of the Promoting First Relationships method in an American Indian community through their tribal Maternal and Child Health program, and to assess the efficacy of the method in this community.

Enrollment

34 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Primary caregiver for a child aged 10 to 30 months
  2. Caregiver lives with the child full time for the past three months and plans to continue for at least 6 more months.
  3. Child is an American Indian or Alaska Native living on or near the Tribe's reservation.
  4. Caregiver has telephone access
  5. Caregiver is willing to have researchers come to their house
  6. Caregiver is English speaking
  7. Caregiver is willing to participate in a home-visiting program which includes video-recorded sessions of caregivers and their children playing

Exclusion Criteria--Caregiver is

  1. hospitalized or imprisoned
  2. living in a Treatment facility or shelter
  3. unable to give consent
  4. live in a household that already has a dyad enrolled in the study.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Wait-List group
Active Comparator group
Description:
Individuals randomized to the control group will receive the intervention program immediately after their 3-month research visit.
Treatment:
Behavioral: Wait-List group
Immediate Group
Experimental group
Description:
Individuals randomized to the Immediate group will receive the intervention program immediately after completing the baseline assessment.
Treatment:
Behavioral: Immediate Group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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