Trial Outcomes & Findings for Engaging Homeless Veterans in Primary Care (NCT NCT00858507)
NCT ID: NCT00858507
Last Updated: 2016-07-21
Results Overview
The primary aim of this study was to conduct a randomized controlled trial of different interventions aimed at increasing rates of treatment engagement among a community sample of treatment-naive homeless veterans.
COMPLETED
NA
221 participants
within 4 weeks of intervention
2016-07-21
Participant Flow
Participant milestones
| Measure |
Arm 1: RN-based Medical Outreach, Administration of a Personal
RN-based medical outreach, administration of a personal health assessment and brief intervention
Personal Health Assessment/brief intervention: RN administered personal health assessment along with a brief intervention for behavior change administered to homeless veterans in the community
|
Arm 2: Social Work Based Outreach (Usual Care)
Social work based outreach (usual care)
Social work administered outreach: Social worker will encounter homeless veteran in the community and encourage to come to the VA for care
|
|---|---|---|
|
Overall Study
STARTED
|
105
|
116
|
|
Overall Study
COMPLETED
|
83
|
101
|
|
Overall Study
NOT COMPLETED
|
22
|
15
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Engaging Homeless Veterans in Primary Care
Baseline characteristics by cohort
| Measure |
Arm 1: RN-based Medical Outreach, Administration of a Personal
n=83 Participants
RN-based medical outreach, administration of a personal health assessment and brief intervention
Personal Health Assessment/brief intervention: RN administered personal health assessment along with a brief intervention for behavior change administered to homeless veterans in the community
|
Arm 2: Social Work Based Outreach (Usual Care)
n=101 Participants
Social work based outreach (usual care)
Social work administered outreach: Social worker will encounter homeless veteran in the community and encourage to come to the VA for care
|
Total
n=184 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
79 Participants
n=5 Participants
|
97 Participants
n=7 Participants
|
176 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
4 Participants
n=5 Participants
|
4 Participants
n=7 Participants
|
8 Participants
n=5 Participants
|
|
Age, Continuous
|
48.8 years
STANDARD_DEVIATION 11.6 • n=5 Participants
|
48.5 years
STANDARD_DEVIATION 10.2 • n=7 Participants
|
48.6 years
STANDARD_DEVIATION 10.8 • n=5 Participants
|
|
Sex: Female, Male
Female
|
6 Participants
n=5 Participants
|
4 Participants
n=7 Participants
|
10 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
77 Participants
n=5 Participants
|
97 Participants
n=7 Participants
|
174 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
83 participants
n=5 Participants
|
101 participants
n=7 Participants
|
184 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: within 4 weeks of interventionThe primary aim of this study was to conduct a randomized controlled trial of different interventions aimed at increasing rates of treatment engagement among a community sample of treatment-naive homeless veterans.
Outcome measures
| Measure |
Arm 1: Outreach
n=83 Participants
RN-based medical outreach, administration of a personal health assessment and brief intervention
Personal Health Assessment/brief intervention: RN administered personal health assessment along with a brief intervention for behavior change administered to homeless veterans in the community
|
Arm 2: Usual Care
n=101 Participants
Social work based outreach (usual care)
Social work administered outreach: Social worker will encounter homeless veteran in the community and encourage to come to the VA for care
|
|---|---|---|
|
Receipt of Primary Care at the VA
|
50 participants
|
39 participants
|
Adverse Events
Arm 1: Outreach
Arm 2: Usual Care
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place