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Impact Of Nurse Navigation Program on Outcomes in Patients With GI Cancers (ACCESS)

Primary Purpose

Gastrointestinal Cancer

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Oncology Nurse Navigation
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Gastrointestinal Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Capable of providing written informed consent and HIPAA authorization for the release of personal health information
  2. Aged ≥ 18 years at the time of consent
  3. Subject is planning to receive their cancer care at LCI at the time of consent
  4. Treatment naïve OR adjuvant greater than 6 months ago, histologically or cytologically confirmed one of the following diagnoses (metastatic/recurrent status can be radiologically confirmed):

    1. Metastatic/recurrent or locally advanced, unresectable or borderline resectable (as defined per NCCN, Alliance or other acceptable guidelines criteria) pancreatic cancer
    2. Metastatic/recurrent or locally advanced, unresectable esophageal, gastroesophageal junction (GEJ) or gastric cancer patients or those who are not eligible for surgery
    3. Metastatic/recurrent or locally advanced, unresectable hepatocellular carcinoma (HCC)

      • radiographic confirmation of the HCC diagnoses is acceptable
      • prior locoregional treatment for subjects with HCC is allowed, but no prior systemic therapy is allowed
    4. Metastatic/recurrent or advanced, unresectable biliary cancers (e.g. gall bladder cancer, cholangiocarcinoma)

      • prior locoregional treatment for subjects with biliary cancers is allowed, but no prior systemic therapy is allowed

    5. Metastatic colorectal or small bowel cancer patients who had disease progression on or are intolerant to fluorouracil/capecitabine, oxaliplatin, and irinotecan-based therapy (e.g. FOLFOX, FOLFIRI or FOLFOXIRI)

      • Subjects can be enrolled within, but no later than 30 days after initiation of their systemic therapy, however every effort will be made to enroll subjects prior to the initiation of systemic therapy. Subjects who has completed or undergoing a current palliative radiotherapy are allowed
  5. As determined by the enrolling physician, ability of the subject to understand and comply with study procedures for the entire length of the study. However, refusal to complete a patient satisfaction questionnaire IL109 should not refrain a subject from being enrolled.
  6. Life expectancy is > 3 months

Exclusion Criteria

  1. Subjects have previously received or are currently receiving LCI Patient Navigation Program services
  2. Subjects with low grade neuroendocrine tumors

Sites / Locations

  • Levine Cancer Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard of Care

Oncology Nurse Navigation

Arm Description

Standard of Care

Standard of Care + Oncology Nurse Navigation

Outcomes

Primary Outcome Measures

Acute Care Utilization
The impact of Oncology Nurse Navigation program on the rate of patient Acute Care Utilization, defined as unplanned inpatient admissions, emergency room encounters, and/or urgent care visits.
Overall Survival
To examine the impact of Oncology Nurse Navigation program on overall survival rate at 6 months.

Secondary Outcome Measures

Oncology Nurse Navigation Comparison Overall Survival
Rate of overall survival and overall survival at 12 months
Oncology Nurse Navigation Comparison Hospital Stay
Compare the length of hospital stay
Oncology Nurse Navigation Comparison Hospice
Time from hospice referral to death
Oncology Nurse Navigation Comparison Readmission Rate
Rate of Readmission after 30 days
Oncology Nurse Navigation Comparison Referral Rate
Rate of referral to Palliative Care, Hospice, Nutrition Services, and Social Work Services
Oncology Nurse Navigation Comparison for Compliance
Rate of adherence to clinical care (the number of no-shows as a percent of all scheduled within Atrium Health, regardless of visit type)
Oncology Nurse Navigation Comparison for Satisfaction
Subject satisfaction assessed by a modified European Organization for Research and Treatment of Cancer Patient Satisfaction with cancer care questionnaire #33 (EORTC PATSAT C33). Scale from 1-5; the higher scores indicates a better outcome

Full Information

First Posted
October 14, 2020
Last Updated
September 26, 2023
Sponsor
Wake Forest University Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT04602611
Brief Title
Impact Of Nurse Navigation Program on Outcomes in Patients With GI Cancers
Acronym
ACCESS
Official Title
A Randomized, Controlled Prospective Trial Evaluating The Impact Of A Nurse Navigation Program on Patients With Gastrointestinal Cancers Undergoing Oncological Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 3, 2020 (Actual)
Primary Completion Date
August 10, 2023 (Actual)
Study Completion Date
October 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to learn about the impact of the Oncology Nurse Navigation program on the frequency of Emergency Department, urgent care visits and inpatient hospital admissions; and overall survival rate at 6 months. The investigators aim to understand if prompt and effective coordination of care provided by Oncology Nurse Navigation (ONN) service will reduce the number of avoidable, unplanned ED visits and hospitalizations, as well as adding measurable value to cancer care, and improve patient overall survival.
Detailed Description
A randomized controlled prospective trial evaluating the effectiveness of a nurse navigation program for gastrointestinal cancer patients undergoing oncological treatment. Upon accrual, patients will be randomized 1:1 to receive standard of care plus ONN service (n = 107) or standard of care only (without ONN service; n = 107). Patients in both arms will be assessed for acute care utilization and overall survival (OS) rate at 6 months. Anticipated accrual period will be 30 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastrointestinal Cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Standard of Care
Arm Title
Oncology Nurse Navigation
Arm Type
Experimental
Arm Description
Standard of Care + Oncology Nurse Navigation
Intervention Type
Other
Intervention Name(s)
Oncology Nurse Navigation
Intervention Description
Providing the subject with the service of navigation (ONN) performed under LCI Patient Navigation Program (LPNP), led by a registered oncology nurse.
Primary Outcome Measure Information:
Title
Acute Care Utilization
Description
The impact of Oncology Nurse Navigation program on the rate of patient Acute Care Utilization, defined as unplanned inpatient admissions, emergency room encounters, and/or urgent care visits.
Time Frame
From the date of randomization until subject is off-intervention, assessed up to 6 months
Title
Overall Survival
Description
To examine the impact of Oncology Nurse Navigation program on overall survival rate at 6 months.
Time Frame
From the date of randomization until 6 months
Secondary Outcome Measure Information:
Title
Oncology Nurse Navigation Comparison Overall Survival
Description
Rate of overall survival and overall survival at 12 months
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison Hospital Stay
Description
Compare the length of hospital stay
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison Hospice
Description
Time from hospice referral to death
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison Readmission Rate
Description
Rate of Readmission after 30 days
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison Referral Rate
Description
Rate of referral to Palliative Care, Hospice, Nutrition Services, and Social Work Services
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison for Compliance
Description
Rate of adherence to clinical care (the number of no-shows as a percent of all scheduled within Atrium Health, regardless of visit type)
Time Frame
From the date of randomization up until 12 months
Title
Oncology Nurse Navigation Comparison for Satisfaction
Description
Subject satisfaction assessed by a modified European Organization for Research and Treatment of Cancer Patient Satisfaction with cancer care questionnaire #33 (EORTC PATSAT C33). Scale from 1-5; the higher scores indicates a better outcome
Time Frame
From the date of randomization up until 12 months
Other Pre-specified Outcome Measures:
Title
Oncology Nurse Navigation Provider Comparison for Outcomes
Description
Outcome comparison for subjects within the ONN arm for subjects navigated by GI specialists versus subjects navigated by general oncology nurse navigators
Time Frame
From the date of randomization until 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Informed consent and HIPAA authorization for the release of personal health information Aged ≥ 18 years at the time of consent Subject is planning to receive their cancer care at LCI at the time of consent Treatment naïve OR adjuvant greater than 6 months ago, histologically or cytologically confirmed one of the following diagnoses (metastatic/recurrent status can be radiologically confirmed): Metastatic/recurrent or locally advanced, unresectable or borderline resectable (as defined per NCCN, Alliance or other acceptable guidelines criteria) pancreatic cancer Metastatic/recurrent or locally advanced, unresectable esophageal, gastroesophageal junction (GEJ) or gastric cancer patients or those who are not eligible for surgery Metastatic/recurrent or locally advanced, unresectable hepatocellular carcinoma (HCC) radiographic confirmation of the HCC diagnoses is acceptable prior locoregional treatment for subjects with HCC is allowed, but no prior systemic therapy is allowed Metastatic/recurrent or advanced, unresectable biliary cancers (e.g. gall bladder cancer, cholangiocarcinoma) • prior locoregional treatment for subjects with biliary cancers is allowed, but no prior systemic therapy is allowed Metastatic colorectal or small bowel cancer patients who had disease progression on or are intolerant to fluorouracil/capecitabine, oxaliplatin, and irinotecan-based therapy (e.g. FOLFOX, FOLFIRI or FOLFOXIRI) Subjects can be enrolled within, but no later than 30 days after initiation of their systemic therapy, however every effort will be made to enroll subjects prior to the initiation of systemic therapy. Subjects who has completed or undergoing a current palliative radiotherapy are allowed Ability to read and understand the English or Spanish language As determined by the enrolling physician, ability of the subject to understand and comply with study procedures for the entire length of the study. However, refusal to complete a patient satisfaction questionnaire IL109 should not refrain a subject from being enrolled. Life expectancy is > 3 months Exclusion Criteria Subjects have previously received or are currently receiving LCI Patient Navigation Program services Subjects with colorectal cancer enrolled in the Empower Program Subjects with low grade neuroendocrine tumors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed Salem, MD
Organizational Affiliation
Wake Forest University Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Levine Cancer Institute
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28204
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Impact Of Nurse Navigation Program on Outcomes in Patients With GI Cancers

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