Health Gatherings - For Your Health After Cancer
Primary Purpose
Prostate Neoplasm, Genital Neoplasms, Male, Urogenital Neoplasms
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cultural CBSM
Standard CBSM
Sponsored by
About this trial
This is an interventional supportive care trial for Prostate Neoplasm focused on measuring prostate cancer, localized prostate cancer, spanish, latino, hispanic, stress management
Eligibility Criteria
Inclusion Criteria:
- ≥ 18 years of age;
- Hispanic/Latino self-identification;
- Spanish speakers (including bilinguals who express interest in a Spanish-based psychosocial intervention);
- Primary diagnosis of localized Prostate Cancer (T1-T3, N0, M0);
- Surgical or radiation treatment (e.g., external beam, brachytherapy, proton) within minimum of 4 months and maximum of 72-months;
- Some patients with prior inpatient psychiatric treatment for severe mental illness or overt signs of severe psychopathology (e.g., psychosis) may be enrolled, per P.I. discretion, based on a case-by-case review;
- Willingness to be randomized and followed for approximately12 months.
Exclusion Criteria:
- History of non-skin cancer within the last 2 years.
- Prior inpatient psychiatric treatment for severe mental illness or overt signs of severe psychopathology (e.g., psychosis) within the past six months, as these conditions can interfere with adequate participation in our experimental conditions may be exclusionary, per P.I. discretion, based on a case-by-case review;
- Active alcohol dependence within the past six months may be exclusionary, per P.I. discretion, based on a case-by-case review;
- Active substance dependence within the past six months may be exclusionary, per P.I. discretion, based on a case-by-case review; and
- Acute or chronic immune system medical conditions, medications or conditions that impact immune and endocrine function (e.g., Chronic Fatigue Syndrome (CFS), Lupus, rheumatoid arthritis, Hepatitis C, or immunosuppressive treatment requiring conditions), per PI discretion based on a case by case review.
Individuals scoring >3 on the SPMSQ will be excluded or per PI discretion based on a case by case review.
.
Sites / Locations
- University of Miami
- Northwestern University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cultural-Cognitive Behavioral Stress Management (CCBSM)
Cognitive Behavioral Stress Management (CBSM)
Arm Description
Participants randomized to this arm will receive 10 weekly group-based C-CBSM intervention.
Participants randomized to this arm will receive 10 weekly group-based standard CBSM intervention.
Outcomes
Primary Outcome Measures
Change in symptom burden as measure by EPIC-S.
Symptom Burden will be measured using the Expanded Prostate Cancer Index Composite (EPIC) - Short Form Summary (EPIC-S). The EPIC-S is a 6-item questionnaire with a total score ranging from 6 - 29 with the lower score indicating greater symptom burden.
Change in HRQoL as measured by the FACT questionnaire.
HRQoL will be measured using Functional Assessment of Cancer Therapy - Prostate (FACT-P) including 4 domains of the FACT-General (FACT-G). The questionnaire has 39 items, with the total score ranging from 0-156. Higher scores indicate better function.
Change in symptom burden as measure by EPIC-UIN.
Symptom Burden will be measured using the EPIC-Short Form Urinary Domain (EPIC-UIN). The EPIC-UIN is a 5-item questionnaire with a total score ranging from 9-43 with the higher score indicating greater symptom burden.
Change in HRQoL as measured by the PROMIS Fatigue questionnaire
HRQoL will be measured using Patient-Reported Outcome Measurement Information System (PROMIS) short form for Fatigue Questionnaire. The total score ranges from 95-475 with the higher score indicating increased fatigue.
Change in HRQoL as measured by the PROMIS Pain questionnaire
HRQoL will be measured using PROMIS short form for Pain Questionnaire. The items are item banks and the scoring via a computer adaptive testes (CAT) which use item response theory (IRT) to calculate a score that is transformed to a T score. Items are administered in an iterative approach where subsequent items are calibrated on prior ones. Once standard error reaches 2 or less, the CAT stops administering items. The higher the score the greater pain symptom.
Secondary Outcome Measures
Change in stress management skills as measured by MOCS-A
Stress management skills will be measured using the Measure of Current Status Part A (MOCS-A) Questionnaire. MOCS-A is a 13-item questionnaire with a total score ranging from 0 - 52 with the higher score indicating greater stress management skills.
Change in prostate cancer-specific psychological distress as measured by MAX-PC - Section I-II
Psychological distress will be measured using the Memorial Anxiety Scale for Prostate Cancer Patients (MAX-PC) Questionnaire. The MAX-PC sections I-II is a 14-item questionnaire with a total score ranging from 0-42 with the higher score indicating increased distress.
Change in prostate cancer-specific psychological distress as measured by MAX-PC - Section III
Psychological distress will be measured using the Memorial Anxiety Scale for Prostate Cancer Patients (MAX-PC) Questionnaire. The MAX-PC section III is a 4-item questionnaire with a total score ranging from 0-12 with the lower score indicating increased distress.
Change in psychosocial distress as measured by the PROMIS Depression questionnaire
PROMIS-Depression is a 28-item questionnaire with a total score ranging from 28-140 with the higher score indicating increased symptoms of depression.
Change in psychosocial distress as measured by the PROMIS Anxiety questionnaire
PROMIS-Anxiety is a 29-item questionnaire with a total score ranging from 29-145 with the higher score indicating increased symptoms of anxiety.
Change in interpersonal function as measured the SIP questionnaire
Sickness Impact Profile (SIP) is a 20-item questionnaire responded with a yes or no. The total number of yes responses will be scored as 1 point with the total score ranging from 0-20 with the higher score indicating poor interpersonal function.
Change in the activation of leukocyte glucocorticoid receptors expression
Leukocyte glucocorticoid receptor expression will be evaluated via blood serum
Change in the inflammatory gene expression
Inflammatory gene expression will be evaluated via blood serum.
Full Information
NCT ID
NCT03344757
First Posted
September 27, 2017
Last Updated
August 14, 2023
Sponsor
University of Miami
Collaborators
Northwestern University, National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT03344757
Brief Title
Health Gatherings - For Your Health After Cancer
Official Title
Culturally Adapted Cognitive Behavioral Stress and Self-Management (C-CBSM) Intervention for Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 5, 2017 (Actual)
Primary Completion Date
August 1, 2024 (Anticipated)
Study Completion Date
August 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Miami
Collaborators
Northwestern University, National Cancer Institute (NCI)
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 look at the effects of a 10-week stress management in-person group program. The program will study emotions, stress, and stress management techniques (such as relaxation and coping techniques) on quality of life, distress, depression, and physical health in Spanish- speaking, Hispanic/Latino men diagnosed with Prostate Cancer (PC).
Detailed Description
This 5-year study evaluates the effects of a 10-week group-based linguistically translated and culturally adapted cognitive-behavioral stress and self-management (C-CBSM) intervention on symptom burden and health related quality of life (HRQoL) in Hispanic men treated for localized prostate cancer (PC). About 80% PC cases are diagnosed as early disease and have a 5- and 10-year survival rate of almost 100% and 99%, respectively.1 Most patients receive active treatment (~70%) leading to prolonged treatment-related side effects and dysfunction persisting well beyond primary treatment. Survival is offset by chronic side effects such as sexual and urinary dysfunction, pain and fatigue that can lead to poor psychosocial functioning, impaired intimacy and social functioning, and masculinity concerns. Hispanic PC survivors report lower physical and social functioning, poorer emotional well-being and greater sexual and urinary dysfunction, even after accounting for SES and disease severity. These sequelae can lead to elevated glucocorticoid release and inflammatory cytokines that have a direct effect on these symptoms and can interfere with physiological pathways necessary for recovery of sexual and urinary functioning. We have shown that CBSM reduces symptom burden and improves HRQoL in bilingual Hispanic PC survivors. In a pilot we showed that a linguistic translation of CBSM with attention to sociocultural processes improved symptom burden and HRQoL in Spanish monolingual PC survivors. We have also shown that CBSM is associated with reduced glucocorticoid resistance and inflammatory gene expression pathways in circulating leukocytes among breast cancer survivors. We propose to (a) deliver a culturally adapted C-CBSM intervention in Spanish that places greater emphasis on salient sociocultural determinants of symptom burden and HRQoL in Hispanics (e.g., fatalistic attitudes, family interdependence, perceived discrimination, machismo), (b) incorporate a neuroimmune model of symptom regulation and management, and (c) test the efficacy of C-CBSM, relative to standard non-culturally adapted CBSM, in two diverse Hispanic communities (Chicago & Miami). We will test our aims in 200 Hispanic men post-treatment for localized PC with elevated symptom burden in a 2 x 4 randomized design with condition (C-CSBM vs. CBSM) as the between groups factors, and time (baseline, post-intervention & 6- and 12-months post intervention) as the within groups factor.
Our Primary Aim is to determine whether randomization to C-CBSM, relative to standard CBSM, is associated with reduced symptom burden and improved HRQoL. Our Secondary Aims evaluate whether C-CBSM leads to greater improvements in the intervention targets (e.g., stress management, psychological distress & interpersonal disruption), and physiologic adaptation (i.e., glucocorticoid receptor sensitivity & inflammatory gene expression). We will also evaluate psychosocial and physiological mechanisms as mediators of C-CBSM's effects on our primary outcomes. We also explore several moderators (e.g., SES, acculturation, treatment, Hispanic origin) of C-CBSM's effect on primary outcomes and the effects of C-CBSM on cardiometabolic health (e.g., lipids, fasting glucose) via reduced inflammation.
Primary Aim 1: Determine whether participation in C-CBSM is associated with significantly greater reductions in symptom burden and improvements in HRQoL relative to participation in CBSM.
Secondary Aims:
Aim 2: Determine whether participation in C-CBSM is associated with significantly greater improvements in intervention targets (i.e., improved stress management, and reduced psychological distress and interpersonal disruption) relative to participation in the CBSM condition.
Aim 3: Determine whether participation in C-CBSM is associated with significantly greater activation of leukocyte glucocorticoid receptor and less inflammatory gene expression profiles relative to CBSM.
Aim 4: Determine whether C-CBSM related improvements in symptom burden and HRQoL are mediated by improvements in intervention targets and gene expression profiles.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Neoplasm, Genital Neoplasms, Male, Urogenital Neoplasms, Neoplasm, Prostate, Genital Diseases, Male, Prostatic Diseases
Keywords
prostate cancer, localized prostate cancer, spanish, latino, hispanic, stress management
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cultural-Cognitive Behavioral Stress Management (CCBSM)
Arm Type
Experimental
Arm Description
Participants randomized to this arm will receive 10 weekly group-based C-CBSM intervention.
Arm Title
Cognitive Behavioral Stress Management (CBSM)
Arm Type
Active Comparator
Arm Description
Participants randomized to this arm will receive 10 weekly group-based standard CBSM intervention.
Intervention Type
Behavioral
Intervention Name(s)
Cultural CBSM
Intervention Description
The Culturally Adapted Cognitive Behavioral Stress Management (C-CBSM) Intervention is a 10 weekly in-person group program. Each session will last about 90 minutes. The meetings will give facts on stress, coping with difficult events, managing anger, social support and stress reactions. Participants will also receive information on how to practice relaxation on their own. The delivery of C-CBSM places a greater emphasis on salient sociocultural determinants of symptom burden and Health Related Quality of Life (HRQoL) in Hispanics (e.g., fatalistic attitudes, family interdependence, perceived discrimination, machismo).
Intervention Type
Behavioral
Intervention Name(s)
Standard CBSM
Intervention Description
The standard Cognitive Behavioral Stress Management (CBSM) Intervention is a 10 weekly in-person group program. Each session will last about 90 minutes. The meetings will give facts on stress, coping with difficult events, managing anger, social support and stress reactions. Participants will also receive information on how to practice relaxation on their own.
Primary Outcome Measure Information:
Title
Change in symptom burden as measure by EPIC-S.
Description
Symptom Burden will be measured using the Expanded Prostate Cancer Index Composite (EPIC) - Short Form Summary (EPIC-S). The EPIC-S is a 6-item questionnaire with a total score ranging from 6 - 29 with the lower score indicating greater symptom burden.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in HRQoL as measured by the FACT questionnaire.
Description
HRQoL will be measured using Functional Assessment of Cancer Therapy - Prostate (FACT-P) including 4 domains of the FACT-General (FACT-G). The questionnaire has 39 items, with the total score ranging from 0-156. Higher scores indicate better function.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in symptom burden as measure by EPIC-UIN.
Description
Symptom Burden will be measured using the EPIC-Short Form Urinary Domain (EPIC-UIN). The EPIC-UIN is a 5-item questionnaire with a total score ranging from 9-43 with the higher score indicating greater symptom burden.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in HRQoL as measured by the PROMIS Fatigue questionnaire
Description
HRQoL will be measured using Patient-Reported Outcome Measurement Information System (PROMIS) short form for Fatigue Questionnaire. The total score ranges from 95-475 with the higher score indicating increased fatigue.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in HRQoL as measured by the PROMIS Pain questionnaire
Description
HRQoL will be measured using PROMIS short form for Pain Questionnaire. The items are item banks and the scoring via a computer adaptive testes (CAT) which use item response theory (IRT) to calculate a score that is transformed to a T score. Items are administered in an iterative approach where subsequent items are calibrated on prior ones. Once standard error reaches 2 or less, the CAT stops administering items. The higher the score the greater pain symptom.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Secondary Outcome Measure Information:
Title
Change in stress management skills as measured by MOCS-A
Description
Stress management skills will be measured using the Measure of Current Status Part A (MOCS-A) Questionnaire. MOCS-A is a 13-item questionnaire with a total score ranging from 0 - 52 with the higher score indicating greater stress management skills.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in prostate cancer-specific psychological distress as measured by MAX-PC - Section I-II
Description
Psychological distress will be measured using the Memorial Anxiety Scale for Prostate Cancer Patients (MAX-PC) Questionnaire. The MAX-PC sections I-II is a 14-item questionnaire with a total score ranging from 0-42 with the higher score indicating increased distress.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in prostate cancer-specific psychological distress as measured by MAX-PC - Section III
Description
Psychological distress will be measured using the Memorial Anxiety Scale for Prostate Cancer Patients (MAX-PC) Questionnaire. The MAX-PC section III is a 4-item questionnaire with a total score ranging from 0-12 with the lower score indicating increased distress.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in psychosocial distress as measured by the PROMIS Depression questionnaire
Description
PROMIS-Depression is a 28-item questionnaire with a total score ranging from 28-140 with the higher score indicating increased symptoms of depression.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in psychosocial distress as measured by the PROMIS Anxiety questionnaire
Description
PROMIS-Anxiety is a 29-item questionnaire with a total score ranging from 29-145 with the higher score indicating increased symptoms of anxiety.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in interpersonal function as measured the SIP questionnaire
Description
Sickness Impact Profile (SIP) is a 20-item questionnaire responded with a yes or no. The total number of yes responses will be scored as 1 point with the total score ranging from 0-20 with the higher score indicating poor interpersonal function.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in the activation of leukocyte glucocorticoid receptors expression
Description
Leukocyte glucocorticoid receptor expression will be evaluated via blood serum
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
Title
Change in the inflammatory gene expression
Description
Inflammatory gene expression will be evaluated via blood serum.
Time Frame
Baseline to Month 3, Baseline to Month 6, Baseline to Month 12
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
≥ 18 years of age;
Hispanic/Latino self-identification;
Spanish speakers (including bilinguals who express interest in a Spanish-based psychosocial intervention);
Primary diagnosis of localized Prostate Cancer (T1-T3, N0, M0);
Surgical or radiation treatment (e.g., external beam, brachytherapy, proton) within minimum of 4 months and maximum of 72-months;
Some patients with prior inpatient psychiatric treatment for severe mental illness or overt signs of severe psychopathology (e.g., psychosis) may be enrolled, per P.I. discretion, based on a case-by-case review;
Willingness to be randomized and followed for approximately12 months.
Exclusion Criteria:
History of non-skin cancer within the last 2 years.
Prior inpatient psychiatric treatment for severe mental illness or overt signs of severe psychopathology (e.g., psychosis) within the past six months, as these conditions can interfere with adequate participation in our experimental conditions may be exclusionary, per P.I. discretion, based on a case-by-case review;
Active alcohol dependence within the past six months may be exclusionary, per P.I. discretion, based on a case-by-case review;
Active substance dependence within the past six months may be exclusionary, per P.I. discretion, based on a case-by-case review; and
Acute or chronic immune system medical conditions, medications or conditions that impact immune and endocrine function (e.g., Chronic Fatigue Syndrome (CFS), Lupus, rheumatoid arthritis, Hepatitis C, or immunosuppressive treatment requiring conditions), per PI discretion based on a case by case review.
Individuals scoring >3 on the SPMSQ will be excluded or per PI discretion based on a case by case review.
.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank Penedo, Ph.D.
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Health Gatherings - For Your Health After Cancer
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