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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03067649
Other study ID # 12112015113639
Secondary ID U.S. NIH/1RC1MH0
Status Completed
Phase N/A
First received February 22, 2017
Last updated April 7, 2017
Start date February 2010
Est. completion date December 2016

Study information

Verified date April 2017
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this study was to test whether conducting a brief motivational interview that focused on perceived barriers to treatment seeking would increase the likelihood that a parent with psychiatric problems would seek treatment for themselves.


Description:

The primary aim of this study was to test a method for increasing adherence to treatment recommendations for parents of children with emotional/behavior problems. Mental health problems in parents can be a serious risk factor for psychiatric and medical problems in children, yet most parents of children receiving services for mental health or medical problems do not get treatment for their own problems. The specific aim of this study was to increase parents' adherence to recommendations for treatment. Parents were randomly assigned to either the Enhanced Motivational Intervention (EMI) or an information only control group. The EMI involves motivational interviewing comprised of a brief intervention that elicits the parents' "story," provides education about their problem(s), describes the potential link between parents' and children's symptoms, assesses their prior treatment history, expectations, and concerns about treatment, identifies potential barriers to treatment seeking, and determines the next step. Evaluations at baseline and 8-weeks and 4-months post intervention will assess parents' symptoms, functioning, and service utilization. The investigators hypothesized that adherence to treatment recommendations would be significantly greater for parents in the EMI group compared to parents in the control group.


Recruitment information / eligibility

Status Completed
Enrollment 194
Est. completion date December 2016
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Parent or guardian of a child who is receiving services for emotional or behavioral problems.

- Must have legal custody of the child

Exclusion Criteria:

- Current psychosis

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Motivational Interview
90-minute interview to discuss their concerns and possible barriers to seeking treatment for themselves
Information only control
Participants are provided with a pamphlet containing referral information

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University National Institutes of Health (NIH)

Outcome

Type Measure Description Time frame Safety issue
Primary Contact a treatment provider Number of participants who contacted a treatment provider by the 4-month post intervention evaluation
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