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Sharing and Talking About my Preferences (STAMPVA)

V

VA Connecticut Healthcare System

Status

Unknown

Conditions

Chronic Disease

Treatments

Behavioral: Motivational Enhancement Therapy
Behavioral: Computer-Tailored Intervention
Behavioral: Motivational Interviewing

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

Details and patient eligibility

About

The purpose of this study is to figure out the best way to help veterans do advance care planning. This study will examine the effects of two theory based behavior interventions by randomizing veteran into 4 groups to see which veterans will complete the 4 step process of advance care planning.

Full description

Purpose: The purpose of this study is to examine the effects of two theory-based behavior interventions on engagement of Veterans in advance care planning (ACP) by means of the following specific aim:

Primary Aim: To conduct a randomized controlled trial examining the effects of: a) usual care; b) computer-tailored intervention (CTI); c) motivational enhancement therapy (MET); d) CTI + MET on the proportion of middle-age and older Veterans receiving primary care at the VA who complete the process of ACP, defined as completing a total of 4 key ACP behaviors, including selecting a health care proxy, communicating with the proxy about goals of care, communicating with the clinician about goals of care, and documenting proxy selection and goals.

Primary Hypothesis: The proportion of Veterans completing ACP will be higher among those in each of the intervention groups compared to Veterans receiving usual care.

All of 4 groups will receive their assessments and, if, their interventions, by telephone and/or mail. The veterans will from the VA Connecticut Healthcare System. Participants will be identified through a data query of the Regional Data Warehouse who have had a primary care visit in the past 12 months. We will then be able to oversample female and minority Veterans.

Enrollment

484 estimated patients

Sex

All

Ages

55+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Veteran

    ---Must have seen primary care provider in the past 12 months

  • Primary language is English

Exclusion criteria

  • Severe hearing or vision loss

    • moderate-to-severe cognitive impairment
  • active psychiatric illness

  • No regular phone or permanent address

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

484 participants in 4 patient groups

Computer-tailored intervention
Active Comparator group
Treatment:
Behavioral: Computer-Tailored Intervention
Motivational Interviewing
Active Comparator group
Treatment:
Behavioral: Motivational Interviewing
Motivational Enhancement Therapy
Active Comparator group
Treatment:
Behavioral: Motivational Enhancement Therapy
Control Group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Maria zenoni, MS; Lynne Iannone, MS

Data sourced from clinicaltrials.gov

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