Pragmatic RCT of SBIRT-PM

NACompletedINTERVENTIONAL
Enrollment

1,101

Participants

Timeline

Start Date

October 23, 2019

Primary Completion Date

April 11, 2024

Study Completion Date

April 11, 2024

Conditions
Substance Use DisordersPain
Interventions
BEHAVIORAL

SBIRT-PM

SBIRT-PM involves an initial telephone-delivered session followed by up to three calls to Veterans in a 12-week period to support Veteran engagement in multi-modal non-pharmacological pain care and to motivate those who misuse substances to change this problematic behavior. SBIRT-PM also includes coordination between the SBIRT-PM clinicians and the PACT nurse case manager after the initial session to support these patient outcomes.

Trial Locations (9)

06520

Yale University, New Haven

06516

VA Connecticut Healthcare System (VACHS), West Haven

04330

VA Maine Healthcare System, Augusta

01730

Edith Nourse Rogers Memorial VA Hospital (VA Bedford), Bedford

02301

VA Boston Healthcare System, Boston

02053

VA Central Western Massachusetts Healthcare System, Leeds

03104

Manchester VA Medical Center, Manchester

02908

Providence VA Medical Center, Providence

05001

White River Junction VA Hospital, White River Junction

All Listed Sponsors
collaborator

National Center for Complementary and Integrative Health (NCCIH)

NIH

collaborator

National Institute on Drug Abuse (NIDA)

NIH

collaborator

US Department of Veterans Affairs

FED

lead

Yale University

OTHER

NCT04062214 - Pragmatic RCT of SBIRT-PM | Biotech Hunter | Biotech Hunter