Vets Helping Vets Pilot Study (VHV)

The overall goal of this study is to evaluate the feasibility of a veteran patient navigator and social work counseling intervention in veterans with advanced stage cancer at the Denver VA Medical Center. This is a tiered intervention: patients first receive the veteran patient navigator component of the intervention, and then if additional patient needs are present they receive the social work counseling component of the intervention. The overall intervention will help veterans communicate their care preferences with their providers.This is a study of behavioral and care strategy interventions and involves no investigational drugs or devices.

Study Overview

Detailed Description

Many patients with advanced cancer suffer from multiple symptoms including pain and fatigue and high rates of depression and anxiety. Many also experience end of life care that is inconsistent with their preferences.

Recent studies of palliative care find that symptoms, depression, and end of life care quality improved in patients with advanced cancer with multidisciplinary, specialist palliative care compared to usual care. However, these palliative care interventions are personnel-intensive and require multiple specialist providers. Because of the costs and limited availability of specialist palliative care providers, these interventions cannot be spread to the large population of patients with advanced cancer. Thus, there is a need for scalable interventions to improve symptoms, depression, and end of life care in this patient population.

Patient navigators, who often belong to the community they serve, have improved rates of cancer screening, follow up on abnormal diagnostic tests, and adherence to chemotherapy regimens. There has been increasing recognition that palliative care is an important part of patient navigation. However, to the best of our knowledge, there have been no studies outside our research program that have examined the effects of a peer navigation intervention to improve palliative care outcomes.

While patient navigators hold promise for improving outcomes in patients with advanced cancer, both psychosocial care needs and documenting future care preferences and goals may be complex. Therefore, the proposed intervention will supplement veteran patient navigators with a social work psychosocial intervention. The goal of the proposed study is to evaluate the feasibility of a stepped care intervention including a veteran patient navigator and social worker.

Study Type

Interventional

Enrollment (Actual)

17

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 108 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Adult (over 18 years of age)
  • Patient has an oncology provider within the VA ECHCS
  • English is patient's primary language
  • Has a reliable telephone
  • Diagnosis of cancer deemed as incurable by oncology provider
  • Oncology provider answers "no" to the question, "Would you be surprised if this patient dies in the next year?"

Exclusion Criteria:

  • Already receiving specialist palliative care or receiving hospice care

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention Arm
All participants are enrolled into the intervention arm and receive the Veteran Patient Navigator and Social Work Intervention.
Each study participant will receive a veteran patient navigator intervention which consists of five study visits consisting of advance care planning, pain/symptom management, and education about hospice and palliative care. When clinically indicated, patients will be referred to a social work intervention providing psychosocial care and support.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Aim 1A. Examine intervention feasibility.
Time Frame: 1 year

The intervention will be feasible if:

A. The participation rate is above 40% and the retention rate is above 60%.

1 year
Aim 1B. Examine intervention feasibility.
Time Frame: 1 year

The intervention will be feasible if:

B. Oncology providers and patient participants find the intervention acceptable as defined by mean ratings of above "somewhat" useful/helpful/satisfied (i.e., above 3 on a 1 to 5 Likert scale, where 5 is "extremely" and 1 is "not at all."

1 year
Aim 1C. Examine intervention feasibility.
Time Frame: 1 year

The intervention will be feasible if:

C. There is less than 10% missing data on patient-reported survey measures.

1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Aim 2A. aTrack intervention process in order to improve the intervention
Time Frame: 1 year

A. Determine patient flow through the intervention and adherence to the study protocol by tracking:

a. number of visits

1 year
Aim 2Ab. Track intervention process in order to improve the intervention
Time Frame: 1 year

A. Determine patient flow through the intervention and adherence to the study protocol by tracking:

b. visit length

1 year
Aim 2Ac. Track intervention process in order to improve the intervention
Time Frame: 1 year

A. Determine patient flow through the intervention and adherence to the study protocol by tracking:

c problem addressed

1 year
Aim 2Ad. Track intervention process in order to improve the intervention
Time Frame: 1 year

A. Determine patient flow through the intervention and adherence to the study protocol by tracking:

d. who is seen by the social worker and why

1 year
Aim 2Ae. Track intervention process in order to improve the intervention
Time Frame: 1 year

A. Determine patient flow through the intervention and adherence to the study protocol by tracking:

e. adherence to the study protocol

1 year
Aim 2B. Track intervention process in order to improve the intervention
Time Frame: 1 year
B. Understand patient and oncology provider reactions through qualitative interviews to the intervention to inform how to improve feasibility or helpfulness.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: David Bekelman, MPH, MD, Eastern Colorado Health Care System, Department of Veterans Affairs, Denver, CO

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2016

Primary Completion (Actual)

April 1, 2017

Study Completion (Actual)

April 1, 2017

Study Registration Dates

First Submitted

November 20, 2015

First Submitted That Met QC Criteria

November 24, 2015

First Posted (Estimate)

November 30, 2015

Study Record Updates

Last Update Posted (Actual)

May 11, 2017

Last Update Submitted That Met QC Criteria

May 9, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 15-2137

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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