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N/A N=86 Treatment

Reintegration: The Role of Spouse Telephone BATTLEMIND Pilot Study

Military Spouses · Support Groups · Stress Disorders · Combat Disorders

Enrolled (actual)
86
Serious AEs
0.0%
Results posted
Jun 2013
Primary outcome: Primary: Spouse Self-report of Depression — 8.9; 7.4; 6.9 units on a scale — p=.003

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Telephone support groups (Behavioral)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Memphis VA Medical Center
Primary completion
Jul 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Spouse Self-report of Depression
8.9; 7.4; 6.9 .003 sig
PRIMARY
Anxiety
8.9; 6.7; 6.7 <.001 sig
PRIMARY
Quality of Marriage
32.7; 31.6; 31.9 .26
SECONDARY
Family Coping
104.3; 104.7; 105.7 .20
SECONDARY
Spouse Social Support
44.0; 46.0; 45.5 .04 sig
SECONDARY
Family Communication
19.9; 20.9; 20.9 .10

Summary

This study will expand the Department of Defense (DoD) one time, face-to-face post deployment BATTLEMIND training for spouses of Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Guard/Reserve service members into year-long, telephone groups focusing on education, skills building and support. The goal is to build spouses' resilience to cope with reintegration, help them serve as a support system for returning service members, and ease the transition for families post-deployment.

Eligibility Criteria

Inclusion Criteria

  • have a spouse who participated in OEF/OIF and is at least 1 month post-deployment;
  • if not married, must have lived as married for at least one year;
  • live with the service member when not deployed;
  • have been a spouse/significant other throughout the service member's deployment period;
  • and have a telephone.

Exclusion Criteria

  • current diagnosis of schizophrenia or other major mental illness;
  • auditory impairment that would make telephone use difficult; or
  • service member refusal of assent for spouse to participate.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00870545). 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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