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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

221 participants

Primary outcome timeframe

within 4 weeks of intervention

Results posted on

2016-07-21

Participant Flow

Participant milestones

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

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 intervention

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.

Outcome measures

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

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Arm 2: Usual Care

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Thomas O'Toole, MD

Providence VA Medical Center

Phone: 4012737100

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place