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N/A N=52 Other

Telephone Coaching of Family Members of Veterans With Substance Abuse Problems

Substance Abuse

Enrolled (actual)
52
Serious AEs
0.0%
Results posted
Jun 2021
Primary outcome: Primary: Number of Veteran's Engaged in Mental Health Care — 7; 5 Participants — p=>.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Coaching (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Sep 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Veteran's Engaged in Mental Health Care
7; 5 >.05

Summary

This project will develop and pilot test an enhanced, telephone "coaching" intervention to help family members concerned about a Veteran of the wars in Iraq or Afghanistan who needs to seek treatment for a substance abuse problem.

Eligibility Criteria

Inclusion Criteria

  • CSO is a sibling, spouse/ intimate partner, or parent of a US military Veteran who served in Iraq or Afghanistan since 2001
  • by the report of the CSO the Veteran of interest has a substance abuse problem that has led to interpersonal, legal, occupational, and/or health related negative consequences
  • the CSO reports that the Veteran is not currently receiving treatment for this problem
  • the CSO has contact 4+times/week and lives with or within 30 min. of the Veteran.

Exclusion Criteria

  • CSO has a SUD (Form 90, see Measures)
  • the Veteran is currently incarcerated
  • the CSO has no computer or other device with Internet access able to view video content
  • the CSO or Veteran likely has a psychotic disorder (CSO report on the MINI) (see Measures)
  • the CSO's involvement in a "coaching" intervention meant to encourage the Veteran to actively consider to seek care places the CSO at risk on a physical or psychological basis
  • Callers who do not have access to a safe phone line will not be referred to the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03246646). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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