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Peer Visitation for OEF/OIF Veterans

Primary Purpose

Polytrauma, Blast Injuries

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Peer Visitation
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Polytrauma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

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

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Peer Visitation Training (Peer Mentor)

Peer Visitation

Arm Description

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

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

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

Patient Health Questionnaire-9 (Depression Screen)
9-item depression screen with possible response options ranging from 9-36, with higher numbers indicating greater depression symptom severity.
Post-Traumatic Stress Disorder Checklist- Military Version (PCL-M)
Measures PTSD symptoms. Possible scores range from 19-95, with higher scores indicating greater symptom severity.
Patient Activation Measure
Measures participante self-efficacy, knowledge of and engagement in health care. Possible scores range from 13-52 with higher scores indicating greater efficacy/knowledge/engagement.
General Anger Level
5-item scale developed for this study. Assesses level of perceived experienced anger in the past month. Possible scores range from 5-35 with higher scores indicating greater levels of anger.

Full Information

First Posted
August 31, 2010
Last Updated
April 6, 2015
Sponsor
US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT01193686
Brief Title
Peer Visitation for OEF/OIF Veterans
Official Title
Evaluating a Peer Visitor Program for OIF/OEF Veterans With Polytrauma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.
Detailed Description
Peer visitation (PV) provides individuals newly dealing with a particular injury/ illness with an opportunity to interact with a peer who has successfully managed a similar condition. Interaction with a successful role model can provide credible social support and information, increase self-efficacy and teach coping strategies, which in turn can engender hope and motivation to engage in treatment and use active coping strategies. In spite of the widespread clinical availability of PV programs, the amount and type of training and clinical/organizational varies widely, and empirical support for their efficacy is limited. The main objective of this project is to test the feasibility of implementing a PV program for OEF/OIF veterans with war-related polytrauma. The proposed study represented a unique opportunity to evaluate three important aspects of peer visitation among OEF/OIF Veterans. Our three hypotheses were: H 1: Veteran Peer Visitors (VPVs) who complete the training will demonstrate successful acquisition of efficacy, knowledge and skills as measured by: (1) pre- and post-tests administered before and after the training; (2) trainer evaluations upon completion of the training, (3) self-evaluation of at least two actual peer visits, and (4) evaluation by two individuals who receive peer visits. H2: VPVs who complete the study will demonstrate increased self-care, improved mood, and increased post-traumatic growth compared to pre-training baseline measures. H 3: Veterans who receive a visit from a VPV will endorse improvement in one or more of the following areas: stress, self-efficacy, activation, mood, ability to make meaning of their experiences, and knowledge of coping options. We used a mixed-methods study to evaluate the feasibility of PV training materials developed in a previous grant to certify 12-18 Veteran Peer Visitors (VPVs). In a prior project, the proposed research team developed the training materials to be tested in this feasibility study, including screening tools to identify appropriate candidates for VPV training, an Instructor manual and a Veteran PV workbook. Two types of participants: Veteran Peer Visitors and Recipients of VPVs were recruited via the Polytrauma Network Site in VISN 20 (Seattle). VPVs were nominated by a clinician to participate and, if enrolled, will undergo 2-day training and will be required to pass a test upon completion of training. Training included a VA Voluntary Services background check, and orientation to the VHA and VA privacy policies. VPVs became official VA volunteers. Each certified VPV was required to provide 1-5 visits to at least two Veterans. Both VPVs and recipients of VPV completed surveys at baseline and upon study completion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polytrauma, Blast Injuries

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Peer Visitation Training (Peer Mentor)
Arm Type
Experimental
Arm Description
Veteran Peer Visitors participated in a 2-day training program and then provide at 1-5 visits to at least 2 recipients.
Arm Title
Peer Visitation
Arm Type
Experimental
Arm Description
Veterans who received at least one visit from a Veteran Peer Visitor.
Intervention Type
Other
Intervention Name(s)
Peer Visitation
Intervention Description
Trained Volunteers will visit OEF/OIF Veterans with Polytrauma Injuries to provide support.
Primary Outcome Measure Information:
Title
Post Traumatic Growth Inventory
Description
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.
Time Frame
Upon completion of study requirements (i.e., visits)
Secondary Outcome Measure Information:
Title
Patient Health Questionnaire-9 (Depression Screen)
Description
9-item depression screen with possible response options ranging from 9-36, with higher numbers indicating greater depression symptom severity.
Time Frame
Upon completion of visits.
Title
Post-Traumatic Stress Disorder Checklist- Military Version (PCL-M)
Description
Measures PTSD symptoms. Possible scores range from 19-95, with higher scores indicating greater symptom severity.
Time Frame
Upon study completion.
Title
Patient Activation Measure
Description
Measures participante self-efficacy, knowledge of and engagement in health care. Possible scores range from 13-52 with higher scores indicating greater efficacy/knowledge/engagement.
Time Frame
Post- Participation
Title
General Anger Level
Description
5-item scale developed for this study. Assesses level of perceived experienced anger in the past month. Possible scores range from 5-35 with higher scores indicating greater levels of anger.
Time Frame
Post- Participation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: Not an OEF/OIF Veteran Under age 18 Non English Speaking Psychiatrically at risk (i.e., uncontrolled psychotic symptoms, active substance abuse or dependence)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rhonda M. Williams, PhD
Organizational Affiliation
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Puget Sound Health Care System Seattle Division, Seattle, WA
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22767074
Citation
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.
Results Reference
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Peer Visitation for OEF/OIF Veterans

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