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A Stepped Care Intervention to Reduce Disparities in Mental Health Services Among Cancer Patients and Caregivers

Primary Purpose

Cancer, Lung, Cancer, Head and Neck

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Stepped-Care Intervention
Enhanced Usual Care
Sponsored by
University of Colorado, Denver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer, Lung

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  1. LC and HNC patients:

    Inclusion Criteria:

    • Newly diagnosed LC and/or HNC (within a month of recruitment date from the date of 1st visit oncology, Ear Nose and Throat (ENT), or radiation clinic visit/consultation upon pathologic tissue diagnosis;
    • LC and/or HNC patients at any stage of diagnosis (Stages 0-IV);
    • Over 18 years old;
    • English and/or Spanish speaking;
    • Medically underserved, as defined by at least one or several of the following:

      1. Low-income: Below 400% of the 2016 Federal poverty levels;
      2. Uninsured: No health insurance (public or private insurance);
      3. Underinsured: e.g.: Public insurance (Medicaid, Medicare exclusive, VA); and/or 10% of annual income on out-of-pocket medical expenses for individuals below 200% of the 2016 Federal poverty levels.

    Exclusion Criteria:

    • Individuals who do not meet eligibility criteria, including individuals who do not speak English or Spanish;
    • Those who refuse treatment at one of three hospital sites;
    • Decisionally-challenged adults with cognitive or personality impairment;
    • Suicidal ideation, or
    • Intoxication (alcohol or drugs) that might interfere with their ability to consent or participate in the study;
    • Individuals from vulnerable populations (e.g., inmates or individuals on probation,
    • homeless,
    • pregnant women, and
    • those with auditory impairment.

    Note: Individuals who become pregnant or develop auditory impairments after they have been randomized to study condition may remain in the study until completion.

  2. Caregivers of LC and/or HNC patients

Inclusion Criteria:

  • Primary caregiver of a newly diagnosed LC and/or HNC patient (per criteria for patients);
  • Over 18 years old;
  • English and/or Spanish speaking;
  • Medically underserved, as defined by at least one or several of the following:

    1. Low-income: Below 400% of the 2016 Federal poverty levels;
    2. Uninsured: No health insurance (public or private insurance);
    3. Underinsured:
  • (c.1) Public insurance (i.e., Medicaid, Medicare exclusive, VA);
  • (c.2) 10% of annual income spent on out-of-pocket medical expenses for individuals below 200% of the 2016 Federal poverty level.

Exclusion criteria:

  • Individuals who do not meet eligibility criteria, including individuals who do not speak English or Spanish [at the discretion of the Site Coordinators upon recruitment];
  • Caregivers of patients who refuse treatment at one of three hospital sites.
  • Decisionally challenged adults with:

    1. cognitive or personality impairment,
    2. suicidal ideation, or
    3. intoxication (alcohol or drugs) that might interfere with their ability to consent or participate in the study [at the discretion of the Site Coordinators upon recruitment or the Counselor during the intervention];
  • Individuals from:

    1. vulnerable populations (e.g., inmates or individuals on probation, homeless,
    2. pregnant women, and
    3. those with auditory impairment [at the discretion of the Site Coordinators upon recruitment]).
    4. Individuals who become pregnant or develop auditory impairments after they have been randomized to study condition may remain in the study until completion.

Sites / Locations

  • Denver Health Medical Center
  • University of Colorado Denver
  • National Jewish Health
  • Saint Joseph Hospital
  • Saint Mary's Hospital and Regional Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Stepped-Care Intervention

Enhanced Usual Care

Arm Description

Intervention strategies are grounded in evidence-based Cognitive Behavioral Therapy (CBT), that includes stress management and relaxation treatment strategies and coping skills training. Treatment strategies have been adapted from the Transactional Model of Stress and Coping (TMSC), a theoretical model that predicts that individuals who are able to cope and adapt to the stress related to cancer treatment or caregiving will report less psychological distress than those unable to cope.

Denver Health, St. Mary's and St. Joseph's hospitals provide supportive mental health care for patients such as printed materials, support groups, crisis counseling, and specialized care (e.g., psychiatric medication). Because the amount of usual mental health care that each patient receives varies at each site, the investigators will standardize and monitor the usual care arm across the three sites with an enhanced usual care condition.

Outcomes

Primary Outcome Measures

Symptoms of Depression-Patients
Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer (CA) Form v1.0 - Depression (30 items). The range is from 8 to 40. Higher score indicates worse outcome (higher depression). Raw scores were used in analyses.
Symptoms of Anxiety-Patients
Patient-Reported Outcomes Measurement Information System, Anxiety (PROMIS-Ca) Form v1.0- Anxiety (22 items). The range of scores is between 8 and 40. The raw scores were used. Higher score corresponds to worse outcome.
Change in Coping-Patients
Coping Self-Efficacy (26 items). Scores can rage from 0 to 260. Higher score corresponds to better outcome.

Secondary Outcome Measures

Change in Coping-Caregivers
Coping Self-Efficacy (26 items). Higher score corresponds to better outcome. Scores can rage from 0 to 260. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Symptoms of Anxiety-Caregivers
PROMIS Form v1.0 - Anxiety (29 items). The range of scores is from 8 to 40. Higher score indicates worse outcome (higher anxiety). Raw scores were used in analyses. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Symptoms of Depression-Caregivers
PROMIS Form v1.0 - Depression (28 items). The range is from 8 to 40. Higher score indicates worse outcome (higher depression). Raw scores were used in analyses. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Health-Related Quality of Life-Patients
FACT-G version 4 (27 items). The range is 0-108. Higher values indicate better QOL.
Perceived Stress-Patients
Perceived Stress Scale (PSS) (14 items). The range of scores is 0-40. Higher values indicate higher stress.
Perceived Stress-Caregivers
Perceived Stress Scale (PSS) (14 items). The range is from 0 to 40. Higher values indicate higher stress.
Caregiving Burden-Caregivers
Zarit Burden Interview (ZBI) (12 items). The range of scores is 0-48. Higher scores represent higher burden.

Full Information

First Posted
December 27, 2016
Last Updated
February 24, 2021
Sponsor
University of Colorado, Denver
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1. Study Identification

Unique Protocol Identification Number
NCT03016403
Brief Title
A Stepped Care Intervention to Reduce Disparities in Mental Health Services Among Cancer Patients and Caregivers
Official Title
A Stepped-Care Intervention to Reduce Disparities in Mental Health Services Among Underserved Lung and Head and Neck Cancer Patients and Their Caregivers
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
April 3, 2017 (Actual)
Primary Completion Date
July 17, 2020 (Actual)
Study Completion Date
July 17, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Colorado, Denver

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
Medically under-served (i.e., low-income, uninsured, underinsured) cancer patients generally encounter significant disparities in accessing care for their mental health needs while undergoing toxic treatments that provide considerable physical and emotional stress. Thus, the investigators propose to adapt evidence-based strategies to a stepped-care intervention model to address the mental health needs of under-served lung cancer (LC) and head and neck cancer (HNC) patients and their caregivers across several levels of symptom severity (e.g., mild, moderate, or severe symptoms of depression and anxiety).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Lung, Cancer, Head and Neck

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Stepped-Care Intervention
Arm Type
Experimental
Arm Description
Intervention strategies are grounded in evidence-based Cognitive Behavioral Therapy (CBT), that includes stress management and relaxation treatment strategies and coping skills training. Treatment strategies have been adapted from the Transactional Model of Stress and Coping (TMSC), a theoretical model that predicts that individuals who are able to cope and adapt to the stress related to cancer treatment or caregiving will report less psychological distress than those unable to cope.
Arm Title
Enhanced Usual Care
Arm Type
Active Comparator
Arm Description
Denver Health, St. Mary's and St. Joseph's hospitals provide supportive mental health care for patients such as printed materials, support groups, crisis counseling, and specialized care (e.g., psychiatric medication). Because the amount of usual mental health care that each patient receives varies at each site, the investigators will standardize and monitor the usual care arm across the three sites with an enhanced usual care condition.
Intervention Type
Behavioral
Intervention Name(s)
Stepped-Care Intervention
Intervention Description
The intervention delivered evidence-based CBT and stress management across eight counseling sessions.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Usual Care
Other Intervention Name(s)
Standard of Care
Intervention Description
Consists of a list of standard mental health resources offered at the participating hospital, local community, or national non-profit organizations.
Primary Outcome Measure Information:
Title
Symptoms of Depression-Patients
Description
Patient-Reported Outcomes Measurement Information System (PROMIS)-Cancer (CA) Form v1.0 - Depression (30 items). The range is from 8 to 40. Higher score indicates worse outcome (higher depression). Raw scores were used in analyses.
Time Frame
6-months
Title
Symptoms of Anxiety-Patients
Description
Patient-Reported Outcomes Measurement Information System, Anxiety (PROMIS-Ca) Form v1.0- Anxiety (22 items). The range of scores is between 8 and 40. The raw scores were used. Higher score corresponds to worse outcome.
Time Frame
6-months
Title
Change in Coping-Patients
Description
Coping Self-Efficacy (26 items). Scores can rage from 0 to 260. Higher score corresponds to better outcome.
Time Frame
6-months
Secondary Outcome Measure Information:
Title
Change in Coping-Caregivers
Description
Coping Self-Efficacy (26 items). Higher score corresponds to better outcome. Scores can rage from 0 to 260. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Time Frame
6-months
Title
Symptoms of Anxiety-Caregivers
Description
PROMIS Form v1.0 - Anxiety (29 items). The range of scores is from 8 to 40. Higher score indicates worse outcome (higher anxiety). Raw scores were used in analyses. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Time Frame
6-months
Title
Symptoms of Depression-Caregivers
Description
PROMIS Form v1.0 - Depression (28 items). The range is from 8 to 40. Higher score indicates worse outcome (higher depression). Raw scores were used in analyses. The number of caregivers randomized and analyzed was 118 and 131 in the enhanced usual care and intervention groups, respectively.
Time Frame
6-months
Title
Health-Related Quality of Life-Patients
Description
FACT-G version 4 (27 items). The range is 0-108. Higher values indicate better QOL.
Time Frame
6-months
Title
Perceived Stress-Patients
Description
Perceived Stress Scale (PSS) (14 items). The range of scores is 0-40. Higher values indicate higher stress.
Time Frame
6-months
Title
Perceived Stress-Caregivers
Description
Perceived Stress Scale (PSS) (14 items). The range is from 0 to 40. Higher values indicate higher stress.
Time Frame
6-months
Title
Caregiving Burden-Caregivers
Description
Zarit Burden Interview (ZBI) (12 items). The range of scores is 0-48. Higher scores represent higher burden.
Time Frame
6-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
LC and HNC patients: Inclusion Criteria: Newly diagnosed LC and/or HNC (within a month of recruitment date from the date of 1st visit oncology, Ear Nose and Throat (ENT), or radiation clinic visit/consultation upon pathologic tissue diagnosis; LC and/or HNC patients at any stage of diagnosis (Stages 0-IV); Over 18 years old; English and/or Spanish speaking; Medically underserved, as defined by at least one or several of the following: Low-income: Below 400% of the 2016 Federal poverty levels; Uninsured: No health insurance (public or private insurance); Underinsured: e.g.: Public insurance (Medicaid, Medicare exclusive, VA); and/or 10% of annual income on out-of-pocket medical expenses for individuals below 200% of the 2016 Federal poverty levels. Exclusion Criteria: Individuals who do not meet eligibility criteria, including individuals who do not speak English or Spanish; Those who refuse treatment at one of three hospital sites; Decisionally-challenged adults with cognitive or personality impairment; Suicidal ideation, or Intoxication (alcohol or drugs) that might interfere with their ability to consent or participate in the study; Individuals from vulnerable populations (e.g., inmates or individuals on probation, homeless, pregnant women, and those with auditory impairment. Note: Individuals who become pregnant or develop auditory impairments after they have been randomized to study condition may remain in the study until completion. Caregivers of LC and/or HNC patients Inclusion Criteria: Primary caregiver of a newly diagnosed LC and/or HNC patient (per criteria for patients); Over 18 years old; English and/or Spanish speaking; Medically underserved, as defined by at least one or several of the following: Low-income: Below 400% of the 2016 Federal poverty levels; Uninsured: No health insurance (public or private insurance); Underinsured: (c.1) Public insurance (i.e., Medicaid, Medicare exclusive, VA); (c.2) 10% of annual income spent on out-of-pocket medical expenses for individuals below 200% of the 2016 Federal poverty level. Exclusion criteria: Individuals who do not meet eligibility criteria, including individuals who do not speak English or Spanish [at the discretion of the Site Coordinators upon recruitment]; Caregivers of patients who refuse treatment at one of three hospital sites. Decisionally challenged adults with: cognitive or personality impairment, suicidal ideation, or intoxication (alcohol or drugs) that might interfere with their ability to consent or participate in the study [at the discretion of the Site Coordinators upon recruitment or the Counselor during the intervention]; Individuals from: vulnerable populations (e.g., inmates or individuals on probation, homeless, pregnant women, and those with auditory impairment [at the discretion of the Site Coordinators upon recruitment]). Individuals who become pregnant or develop auditory impairments after they have been randomized to study condition may remain in the study until completion.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Evelinn A Borrayo, PhD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
Denver Health Medical Center
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
University of Colorado Denver
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
National Jewish Health
City
Denver
State/Province
Colorado
ZIP/Postal Code
80206
Country
United States
Facility Name
Saint Joseph Hospital
City
Denver
State/Province
Colorado
ZIP/Postal Code
80218
Country
United States
Facility Name
Saint Mary's Hospital and Regional Medical Center
City
Grand Junction
State/Province
Colorado
ZIP/Postal Code
81502
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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A Stepped Care Intervention to Reduce Disparities in Mental Health Services Among Cancer Patients and Caregivers

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