Internet-Based Exercise and Diet Support in Prostate Cancer Survivors
Primary Purpose
Cancer Survivor, Prostate Carcinoma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Written Information
Prescription
Technology
Coaching
Sponsored by

About this trial
This is an interventional treatment trial for Cancer Survivor
Eligibility Criteria
Inclusion Criteria:
- Self-reported prostate cancer diagnosis
- Able to read English on a computer screen
- Able to access a computer, tablet or smartphone at home or public location
- Access to a device capable of receiving plain text messages
- A personal email address
Exclusion Criteria:
Men who have contraindications to exercise based the American College of Sports Medicine 2016 Exercise pre-participation screening criteria and who do not receive a physician clearance to participate in the moderate intensity physical activity with one or more of the following self-reported conditions:
- heart attack
- heart surgery, cardiac catheterization, or coronary angioplasty
- pacemaker/implantable cardiac defibrillator/rhythm disturbance
- heart valve disease
- heart failure
- heart transplantation
- congenital heart disease
- diabetes
- kidney (renal) disease
- chest discomfort with exertion
- unreasonable breathlessness
- dizziness, fainting or blackouts
- ankle swelling
- unpleasant awareness of forceful, rapid or irregular heart rate
- burning or cramping sensations in your lower legs when walking short distance
Sites / Locations
- UCSF Medical Center-Mount Zion
- Oregon Health & Science University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Experimental
Experimental
Experimental
Arm Label
Group I
Group II
Group III
Group IV
Arm Description
Written Information
Written Information Prescription
Written Information Prescription Technology
Written Information Prescription Technology Coaching
Outcomes
Primary Outcome Measures
Accrual success
Measured as ability to recruit target sample size within one year
Retention
Measured as the % of men who complete post-intervention and follow-up measures out of the total # of men enrolled
Adherence to the study
Measured as the # of times that a man visits the portal over three months
Secondary Outcome Measures
Community Healthy Activities Model Program for Seniors (CHAMPS) physical activity survey
CHAMPS estimates total weekly energy expenditure (in kilocalories per week) from low to vigorous intensity physical activities for older adults.
Harvard T.H. Chan School of Public Health Food Frequency Questionnaire for adults from 2007
This 132-item survey assesses dietary intake over the past month in categories from "never or less than once per month" to "6 or more times per day" and supports examining major food and nutrient categories of the U.S. diet.
Self-Efficacy for Exercise
A 6-item measure of Self-efficacy for Exercise will be used. Summed scores range from 6-30, and higher scores indicate higher self-efficacy.
Physical Activity Stage Assessment
This 5-question measure asks the person to select one description, from a choice of five, which describes his current activity behavior.
Charlson Comorbidity Index
The Charlson Comorbidity Index is a weighted index to predict mortality. Scores range from 0-37, with higher scores indicating more chronic medical conditions.
Self-Efficacy for Diet
Diet self-efficacy will be measured by having participants rate their confidence in performing each recommended task (e.g., two more servings of cooked tomatoes per week) using a Likert scale.
Pittsburgh Sleep Quality Index
This self-report questionnaire assesses sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven "component" scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for these seven components yields one global score.
Memorial Anxiety Scale for Prostate Cancer (MAX-PC)
MAX-PC is an 18 item scale to facilitate the identification and assessment of men with prostate cancer-related anxiety. This scale consists of three subscales that measure general prostate cancer anxiety, anxiety related to prostate specific antigen (PSA) levels in particular, and fear of recurrence.
PROMIS 7-item Short Form - Fatigue
PROMIS - Fatigue evaluates self-reported symptoms of fatigue, from mild subjective feelings of tiredness to an overwhelming sense of exhaustion over the past seven days.
Behavioral Regulation in Exercise Questionnaire (BREQ2)
BREQ2 measures the continuum of behavioral regulation in exercise psychology research. This questionnaire concerns the reasons why a person exercises regularly, works out, or engages in other such physical activities. It is structured so that it asks one question and provides responses that represent external regulation, introjected regulation, identified regulation, and intrinsic motivation.
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)
EORTC QLQ-C30 is a 30-item questionnaire developed to assess the quality of life of cancer patients and has five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea and vomiting), a global health status / QoL scale, and a number of single items assessing additional symptoms commonly reported by cancer patients (dyspnea, loss of appetite, insomnia, constipation and diarrhea) and perceived financial impact of the disease. Scores range from 0-100, with higher functional scale scores indicating a higher level of healthy functioning while a higher score for a symptom scale represents a higher level of symptomatology or problems.
Full Information
NCT ID
NCT03406013
First Posted
July 22, 2017
Last Updated
July 27, 2020
Sponsor
OHSU Knight Cancer Institute
Collaborators
Movember Foundation
1. Study Identification
Unique Protocol Identification Number
NCT03406013
Brief Title
Internet-Based Exercise and Diet Support in Prostate Cancer Survivors
Official Title
True NTH Community of Wellness Internet-Based Exercise and Diet Support for Prostate Cancer Survivors
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
March 31, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
OHSU Knight Cancer Institute
Collaborators
Movember Foundation
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
This pilot clinical trial studies how well the True NTH Community of Wellness internet-based exercise and diet support works in improving diet and exercise habits in prostate cancer survivors. Internet-based exercise and diet support may help better control treatment-related side effects and symptoms, better overall quality of life, and lower risk factors associated with cancer progression.
Detailed Description
PRIMARY OBJECTIVES:
I. To determine the feasibility and acceptability of the Community of Wellness web portal among prostate cancer survivors by conducting a randomized controlled study comparing four levels of web-based content and interaction with participants.
SECONDARY OBJECTIVES:
I. To compare efficacy of four levels of web-based content in the Community of Wellness web portal in a pilot randomized controlled trial on exercise and dietary habits, self-efficacy for behavior change, motivation for exercise, and changes in treatment-related side effects.
OUTLINE: Patients are assigned to 1 of 4 groups.
GROUP I: Patients receive "Written Information" which includes access to the TrueNTH open access portal that provides basic written information about exercise and diet.
GROUP II: Patients receive access to "Written Information + Prescription", including written information plus additional an exercise prescription and tailored diet recommendations.
GROUP III: Patients receive access to "Written Information + Prescription + Technology", including written information, exercise prescription + diet recommendation and additional technology components. Patients complete diet and exercise behavior logs and receive educational and motivational text messages about healthy diet and exercise habits.
GROUP IV: Patients receive access to "Written Information + Prescription + Technology + Coaching" and receive written information, exercise prescription + diet recommendation, technology support and a 30-minute (each) diet and exercise consultation plus the ability to receive ongoing advice from coaches via the web portal.
After completion of intervention, patients are followed up at 3 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer Survivor, Prostate Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
206 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group I
Arm Type
Active Comparator
Arm Description
Written Information
Arm Title
Group II
Arm Type
Experimental
Arm Description
Written Information Prescription
Arm Title
Group III
Arm Type
Experimental
Arm Description
Written Information Prescription Technology
Arm Title
Group IV
Arm Type
Experimental
Arm Description
Written Information Prescription Technology Coaching
Intervention Type
Behavioral
Intervention Name(s)
Written Information
Intervention Description
Receive written information on diet and exercise relevant to older men with prostate cancer
Intervention Type
Behavioral
Intervention Name(s)
Prescription
Intervention Description
Participants receive tailored exercise prescription and tailored diet recommendations
Intervention Type
Behavioral
Intervention Name(s)
Technology
Intervention Description
Participants receive motivational text messages and can electronically log and track their exercise and diet habits
Intervention Type
Behavioral
Intervention Name(s)
Coaching
Intervention Description
Participants receive access to an exercise and diet coach to provide advice by phone and/or email
Primary Outcome Measure Information:
Title
Accrual success
Description
Measured as ability to recruit target sample size within one year
Time Frame
Up to 3 months
Title
Retention
Description
Measured as the % of men who complete post-intervention and follow-up measures out of the total # of men enrolled
Time Frame
Up to 6 months
Title
Adherence to the study
Description
Measured as the # of times that a man visits the portal over three months
Time Frame
Up to 3 months
Secondary Outcome Measure Information:
Title
Community Healthy Activities Model Program for Seniors (CHAMPS) physical activity survey
Description
CHAMPS estimates total weekly energy expenditure (in kilocalories per week) from low to vigorous intensity physical activities for older adults.
Time Frame
Baseline, 3 months, and 6 months
Title
Harvard T.H. Chan School of Public Health Food Frequency Questionnaire for adults from 2007
Description
This 132-item survey assesses dietary intake over the past month in categories from "never or less than once per month" to "6 or more times per day" and supports examining major food and nutrient categories of the U.S. diet.
Time Frame
Baseline, 3 months, and 6 months
Title
Self-Efficacy for Exercise
Description
A 6-item measure of Self-efficacy for Exercise will be used. Summed scores range from 6-30, and higher scores indicate higher self-efficacy.
Time Frame
Baseline, 3 months, and 6 months
Title
Physical Activity Stage Assessment
Description
This 5-question measure asks the person to select one description, from a choice of five, which describes his current activity behavior.
Time Frame
Baseline, 3 months, and 6 months
Title
Charlson Comorbidity Index
Description
The Charlson Comorbidity Index is a weighted index to predict mortality. Scores range from 0-37, with higher scores indicating more chronic medical conditions.
Time Frame
Baseline, 3 months, and 6 months
Title
Self-Efficacy for Diet
Description
Diet self-efficacy will be measured by having participants rate their confidence in performing each recommended task (e.g., two more servings of cooked tomatoes per week) using a Likert scale.
Time Frame
Baseline, 3 months, and 6 months
Title
Pittsburgh Sleep Quality Index
Description
This self-report questionnaire assesses sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven "component" scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for these seven components yields one global score.
Time Frame
Baseline, 3 months, and 6 months
Title
Memorial Anxiety Scale for Prostate Cancer (MAX-PC)
Description
MAX-PC is an 18 item scale to facilitate the identification and assessment of men with prostate cancer-related anxiety. This scale consists of three subscales that measure general prostate cancer anxiety, anxiety related to prostate specific antigen (PSA) levels in particular, and fear of recurrence.
Time Frame
Baseline, 3 months, and 6 months
Title
PROMIS 7-item Short Form - Fatigue
Description
PROMIS - Fatigue evaluates self-reported symptoms of fatigue, from mild subjective feelings of tiredness to an overwhelming sense of exhaustion over the past seven days.
Time Frame
Baseline, 3 months, and 6 months
Title
Behavioral Regulation in Exercise Questionnaire (BREQ2)
Description
BREQ2 measures the continuum of behavioral regulation in exercise psychology research. This questionnaire concerns the reasons why a person exercises regularly, works out, or engages in other such physical activities. It is structured so that it asks one question and provides responses that represent external regulation, introjected regulation, identified regulation, and intrinsic motivation.
Time Frame
Baseline, 3 months, and 6 months
Title
European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30)
Description
EORTC QLQ-C30 is a 30-item questionnaire developed to assess the quality of life of cancer patients and has five functional scales (physical, role, cognitive, emotional, and social), three symptom scales (fatigue, pain, and nausea and vomiting), a global health status / QoL scale, and a number of single items assessing additional symptoms commonly reported by cancer patients (dyspnea, loss of appetite, insomnia, constipation and diarrhea) and perceived financial impact of the disease. Scores range from 0-100, with higher functional scale scores indicating a higher level of healthy functioning while a higher score for a symptom scale represents a higher level of symptomatology or problems.
Time Frame
Baseline, 3 months, and 6 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Self-reported prostate cancer diagnosis
Able to read English on a computer screen
Able to access a computer, tablet or smartphone at home or public location
Access to a device capable of receiving plain text messages
A personal email address
Exclusion Criteria:
Men who have contraindications to exercise based the American College of Sports Medicine 2016 Exercise pre-participation screening criteria and who do not receive a physician clearance to participate in the moderate intensity physical activity with one or more of the following self-reported conditions:
heart attack
heart surgery, cardiac catheterization, or coronary angioplasty
pacemaker/implantable cardiac defibrillator/rhythm disturbance
heart valve disease
heart failure
heart transplantation
congenital heart disease
diabetes
kidney (renal) disease
chest discomfort with exertion
unreasonable breathlessness
dizziness, fainting or blackouts
ankle swelling
unpleasant awareness of forceful, rapid or irregular heart rate
burning or cramping sensations in your lower legs when walking short distance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kerri Winters-Stone
Organizational Affiliation
OHSU Knight Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCSF Medical Center-Mount Zion
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
Facility Name
Oregon Health & Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
33382378
Citation
Chan JM, Van Blarigan EL, Langlais CS, Zhao S, Ramsdill JW, Daniel K, Macaire G, Wang E, Paich K, Kessler ER, Beer TM, Lyons KS, Broering JM, Carroll PR, Kenfield SA, Winters-Stone KM. Feasibility and Acceptability of a Remotely Delivered, Web-Based Behavioral Intervention for Men With Prostate Cancer: Four-Arm Randomized Controlled Pilot Trial. J Med Internet Res. 2020 Dec 31;22(12):e19238. doi: 10.2196/19238.
Results Reference
derived
PubMed Identifier
30442638
Citation
Winters-Stone KM, Kenfield SA, Van Blarigan EL, Moe EL, Ramsdill JW, Daniel K, Macaire G, Paich K, Kessler ER, Kucuk O, Gillespie TW, Lyons KS, Beer TM, Broering JM, Carroll PR, Chan JM. Effect of Increasing Levels of Web-Based Behavioral Support on Changes in Physical Activity, Diet, and Symptoms in Men With Prostate Cancer: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2018 Nov 15;7(11):e11257. doi: 10.2196/11257.
Results Reference
derived
Learn more about this trial
Internet-Based Exercise and Diet Support in Prostate Cancer Survivors
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