NCT01193686

Brief Summary

The goal of this study was to train OIF/OIF Veterans with multiple injuries to be Peer Visitors, i.e., Volunteers who visit more recently OIF/OEF Veterans and provide support. We evaluated the effectiveness of the training, and any benefits that Volunteer Peer Visitors and the Recipients of Peer Visitors experienced as a result of participating in Peer Visitation.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2010

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 31, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 2, 2010

Completed
2 months until next milestone

Study Start

First participant enrolled

November 1, 2010

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2012

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2012

Completed
2.6 years until next milestone

Results Posted

Study results publicly available

January 5, 2015

Completed
Last Updated

April 28, 2015

Status Verified

October 1, 2014

Enrollment Period

1.3 years

First QC Date

August 31, 2010

Results QC Date

December 11, 2014

Last Update Submit

April 6, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • Post Traumatic Growth Inventory

    Administered only to Peer Visitors, possible range 0-105, with higher scores indicating greater post-traumatic growth. Post-traumatic growth includes emotional changes such as noticing a stronger sense of self, deepened relationships, increased sense of gratitude or appreciation for life, increased spirituality.

    Upon completion of study requirements (i.e., visits)

Secondary Outcomes (4)

  • Patient Health Questionnaire-9 (Depression Screen)

    Upon completion of visits.

  • Post-Traumatic Stress Disorder Checklist- Military Version (PCL-M)

    Upon study completion.

  • Patient Activation Measure

    Post- Participation

  • General Anger Level

    Post- Participation

Study Arms (2)

Peer Visitation Training (Peer Mentor)

EXPERIMENTAL

Veteran Peer Visitors participated in a 2-day training program and then provide at 1-5 visits to at least 2 recipients.

Other: Peer Visitation

Peer Visitation

EXPERIMENTAL

Veterans who received at least one visit from a Veteran Peer Visitor.

Other: Peer Visitation

Interventions

Trained Volunteers will visit OEF/OIF Veterans with Polytrauma Injuries to provide support.

Peer VisitationPeer Visitation Training (Peer Mentor)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • For Peer Visitors:
  • eligibility will be determined using a combination of self-assessment, clinician recommendation, and Voluntary Services screening
  • For participants who are interested in receiving a peer visitor:
  • eligibility will be determined by the referring clinical team and the Research Nurse
  • Peer Visitors:
  • To be eligible to participate in the study as a potential Veteran Peer Visitor, Veterans must complete several screening steps. A Veteran must be nominated by a clinician from the Center for Polytrauma Care (CPC) Clinical Team, or they must nominate themselves for the project and seek endorsement from a clinician on the CPC team. To be nominated or endorsed by a clinician, the Veteran must have been observed by the clinical team member to demonstrate the following specific behaviors and characteristics:
  • Reliable and organized about keeping appointments (80% adherence or better)
  • Demonstrate excellent insight into own treatment goals, progress, barriers, treatment rationale
  • Not demonstrate any "high-risk" behaviors in the previous 12 months, including suicidal ideation or intent, inpatient psychiatric treatment (other than planned, voluntary admission to Evaluation and Brief Treatment Unit), active substance abuse or dependence, uncontrolled psychotic symptoms (e.g., hallucinations, delusions), felonies.
  • Evidence of good social support (i.e., clinician aware of supportive relationships)
  • Engaged in meaningful life goals and activities (e.g., work, school, volunteering, parenting, recreation, church)
  • Able to pass background check for Voluntary Services
  • Must be English Speaking
  • Able to complete pen and paper surveys

You may not qualify if:

  • Not an OEF/OIF Veteran
  • Under age 18
  • Non English Speaking
  • Psychiatrically at risk (i.e., uncontrolled psychotic symptoms, active substance abuse or dependence)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

VA Puget Sound Health Care System Seattle Division, Seattle, WA

Seattle, Washington, 98108, United States

Location

Related Publications (1)

  • Williams RM, Bambara J, Turner AP. A scoping study of one-to-one peer mentorship interventions and recommendations for application with Veterans with postdeployment syndrome. J Head Trauma Rehabil. 2012 Jul-Aug;27(4):261-73. doi: 10.1097/HTR.0b013e3182585cb6.

MeSH Terms

Conditions

Multiple TraumaBlast Injuries

Condition Hierarchy (Ancestors)

Wounds and InjuriesBarotrauma

Limitations and Caveats

We had great difficulty recruiting Recipients of Peer Visitors, i.e., Veterans who wished to receive mentorship from our trained peer visitors. This rendered our sample size too small for planned analyses.

Results Point of Contact

Title
Rhonda Williams, Ph.D.
Organization
VA Puget Sound Health Care System

Study Officials

  • Rhonda M. Williams, PhD

    VA Puget Sound Health Care System Seattle Division, Seattle, WA

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 31, 2010

First Posted

September 2, 2010

Study Start

November 1, 2010

Primary Completion

March 1, 2012

Study Completion

June 1, 2012

Last Updated

April 28, 2015

Results First Posted

January 5, 2015

Record last verified: 2014-10

Locations