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Daughters, dUdes, Mothers and othErs Fighting Cancer Together (DUET)

Primary Purpose

Cancer, Overweight and Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
eHealth Intervention
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cancer focused on measuring cancer survivor, overweight, obesity

Eligibility Criteria

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

Inclusion Criteria:

  • Adults age 18+ for whom at least one dyad member has been diagnosed and completed curative treatment for localized renal cancer, or loco-regional ovarian, colorectal, endometrial, or female breast cancer. (Loco-regional prostate cancer survivors are also eligible but could be on active surveillance).
  • Diagnosed as overweight or obese (BMI >25 kg/m2.
  • Low vegetable and fruit intake (<2.5 cups day).
  • Low physical activity (<150 minutes per week).
  • English-speaking and writing.
  • Completed at least 5th grade.
  • Uses the internet and owns a mobile phone.

Exclusion Criteria:

  • Diagnosed with uncontrolled chronic conditions (i.e., diabetes, blood pressure, CVD, etc)
  • Diagnosed with a health conditions that precludes adherence to an unsupervised weight loss intervention (e.g., pregnancy, end-stage renal disease, etc).
  • Instructed by a physician to limit physical activity AND have paralysis, dementia, blindness, unstable angina, untreated stage 3 hypertension, or recent history of heart attack, congestive heart failure or pulmonary conditions that required oxygen or hospitalization within 6 months.
  • Diagnosed with other cancers (except non-malignant skin cancer), cancer recurrence or metastatic disease.
  • Resides in a skilled nursing or assisted living facility.
  • Resides more than 15 minute driving distance from dyad partner.

Sites / Locations

  • UAB School of Health Professions, Department of Nutrition Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Immediate Intervention Group

Delayed Intervention Group

Arm Description

Dyads randomized to the Immediate Intervention Group will receive a "Welcome Box" at completion of the baseline assessment. The Welcome Box will include two of each of the following: 1) Letters describing the project logistics and the important roles of each dyad member); 2) WiFi-enabled Scales (with instructions to weigh daily); 3) Portion Doctor ®Tableware (with instructions to use the portion plates at least once a day); 4) Fitbit® Inspire Activity Monitors (with instructions to share data with the dyad member and the study office); and 5) Instructions on how to create a secured account on the DUET website and instructions for logging on.

Participants assigned to the Delayed Intervention Group will receive a "Welcome Box" which on the outside is identical (and also is comparably weighted with bottled water) to that given to the Immediate Intervention group. This box would include: 1) Letters describing the project logistics and the important roles of each dyad member; and 2) monthly online study newsletters on topics unrelated to diet and exercise, but still of interest to cancer survivors and dyad members such as coping with stress, reducing exposure to radiation, sun safety, etc. to enhance retention and will be offered the opportunity to receive the online intervention after completing final 6-month assessments.

Outcomes

Primary Outcome Measures

Body Weight
Change in measured body weight
Body Weight
Change in measured body weight

Secondary Outcome Measures

Waist Circumference
measured with a non-stretch tape
Waist Circumference
measured with a non-stretch tape
Physical Activity (self-reported)
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Physical Activity (self-reported)
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Physical Activity (self-reported)
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Physical Activity (objective)
Accelerometry (7-day assessment)
Physical Activity (objective)
Accelerometry (7-day assessment)
Diet Quality
Two 24-hour dietary recalls
Diet Quality
Two 24-hour dietary recalls
Physical Performance (endurance)
2-minute step test
Physical Performance (endurance)
2-minute step test
Physical Performance (lower body strength)
30-second chair stand
Physical Performance (lower body strength)
30-second chair stand
Physical Performance (agility)
8' foot up and go
Physical Performance (agility)
8' foot up and go
Physical Performance (gait speed)
8' walk
Physical Performance (gait speed)
8' walk
Physical Performance (Balance)
Side-by-side, semi-tandem and tandem stances
Physical Performance (Balance)
Side-by-side, semi-tandem and tandem stances
Self-efficacy for calorically restricted diet
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Self-efficacy for calorically restricted diet
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Self-efficacy for calorically restricted diet
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Self-efficacy for increased physical activity
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Self-efficacy for increased physical activity
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Self-efficacy for increased physical activity
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Social support for calorically restricted diet
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Social support for increased physical activity
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Social support for calorically restricted diet
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Social support for increased physical activity
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Social support for calorically restricted diet
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Social support for increased physical activity
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Barriers for increased physical activity
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Barriers for increased physical activity
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Barriers for increased physical activity
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Circulating insulin
assays on dried blood spot eluents
Circulating insulin
assays on dried blood spot eluents
Circulating glucose
assays on dried blood spot eluents
Circulating glucose
assays on dried blood spot eluents
Circulating IL-6
assays on dried blood spot eluents
Circulating IL-6
assays on dried blood spot eluents
Circulating CRP
assays on dried blood spot eluents
Circulating CRP
assays on dried blood spot eluents
Circulating Total Cholesterol
assays on dried blood spot eluents
Circulating Total Cholesterol
assays on dried blood spot eluents
Circulating HDL Cholesterol
assays on dried blood spot eluents
Circulating HDL Cholesterol
assays on dried blood spot eluents
Circulating Tryglycerides
assays on dried blood spot eluents
Circulating Tryglycerides
assays on dried blood spot eluents
Circulating Adiponectin
assays on dried blood spot eluents
Circulating Adiponectin
assays on dried blood spot eluents
Circulating Leptin
assays on dried blood spot eluents
Circulating Leptin
assays on dried blood spot eluents
Duke OARS Co-Morbidity Index
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
Duke OARS Co-Morbidity Index
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
Duke OARS Co-Morbidity Index
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
PROMIS v.1.2 GLOBAL HEALTH
10-item Likert scale assessment of Quality of Life
PROMIS v.1.2 GLOBAL HEALTH
10-item Likert scale assessment of Quality of Life
PROMIS v.1.2 GLOBAL HEALTH
10-item Likert scale assessment of Quality of Life
EQ-5D-5L
6-item Likert scale assessment of Quality of Life
EQ-5D-5L
6-item Likert scale assessment of Quality of Life
EQ-5D-5L
6-item Likert scale assessment of Quality of Life
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
7-item scale to assess e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
7-item scale to assess health and e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
7-item scale to assess health and e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
Barriers to Eating a Healthy Low Calorie Diet
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
Barriers to Eating a Healthy Low Calorie Diet
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
Barriers to Eating a Healthy Low Calorie Diet
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
PROMIS Emotional Distress: Depression - Short Form 8a
(8 items) Likert scale assessment of depression
PROMIS Emotional Distress: Depression - Short Form 8a
(8 items) Likert scale assessment of depression
PROMIS Emotional Distress: Depression - Short Form 8a
(8 items) Likert scale assessment of depression
Smoking status
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.
Smoking status
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.
Smoking status
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.

Full Information

First Posted
October 11, 2019
Last Updated
December 13, 2022
Sponsor
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT04132219
Brief Title
Daughters, dUdes, Mothers and othErs Fighting Cancer Together
Acronym
DUET
Official Title
Daughters, (dUdes), Mothers and othErs Fighting Cancer Together
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
October 15, 2020 (Actual)
Primary Completion Date
February 15, 2022 (Actual)
Study Completion Date
February 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham

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 protocol is to conduct a 2-arm, single-blinded randomized controlled clinical trial (RCT) in which 56 dyads (defined as consisting of an overweight or obese cancer survivor of an obesity-related cancer and an overweight or obese "buddy" of his or her choosing) would be assigned either to a 6-month, diet- and exercise-based weight loss intervention delivered via an interactive website with tailored text messages, or to a 6-month wait-listed control group. The overall goals of the eHealth intervention are to reduce obesity and select circulating biomarkers (tumor necrosis factor alpha [TNFα], insulin, and insulin-like growth factor-1 [IGF-1]), as well as improve diet quality, physical activity, health-related quality of life (QoL), physical functioning and performance as compared to the control over the 6-month study period.
Detailed Description
The specific aims of this protocol are to: 1) determine whether dyads (comprised of an overweight / obese cancer survivor and an overweight / obese buddy of his or her choosing) lose significantly more weight (kg) at 6-months when assigned to the eHealth intervention compared to a wait-listed control; 2) explore between-arm differences in score changes between baseline and 6-month follow-up for other key outcomes including measures of adiposity (e.g., waist circumference [WC] and body mass index [BMI]), blood pressure, diet quality, physical activity, health-related Quality of Life (QoL), physical functioning and performance; 3) Assess the impact of the intervention on select biomarkers associated with cancer risk and progression, e.g., tumor TNFα, insulin and IGF-1; and, 4) identify predictor variables associated with program efficacy, e.g., social support, self-efficacy, risk for depression, and dyad partner (spouse, relative, friend/neighbor). Cancer survivors and their selected "buddies" who are interested in participating will be directed to a website that describes this study in detail. If interested, they will be asked to complete an online screener requiring information on race/ethnicity, gender, state of residence and eligibility criteria. Once interested participants are assessed for eligibility, consented and enrolled, they will be asked to complete online questionnaires that assess physical activity, dietary intake, health-related quality of life, risk for depression, self-efficacy, social support and barriers to diet resources. Finally, anthropometric measures, blood pressure, physical performance and circulating biomarkers will be collected in participants' homes by visiting study staff (whom the project manager will deploy after checking for a mutually convenient time for the 2-person dyad.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Overweight and Obesity
Keywords
cancer survivor, overweight, obesity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
We anticipate enrolling 56 dyads of participants (2 per dyad). Each dyad will be randomized to either receive the intervention for 6 months or be placed on a 6-month waitlist and offered the opportunity to try the online intervention after final assessments are completed.
Masking
InvestigatorOutcomes Assessor
Masking Description
Assessors of anthropometric, physical function, patient reported outcomes and biospecimens are blinded to arm status
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Immediate Intervention Group
Arm Type
Experimental
Arm Description
Dyads randomized to the Immediate Intervention Group will receive a "Welcome Box" at completion of the baseline assessment. The Welcome Box will include two of each of the following: 1) Letters describing the project logistics and the important roles of each dyad member); 2) WiFi-enabled Scales (with instructions to weigh daily); 3) Portion Doctor ®Tableware (with instructions to use the portion plates at least once a day); 4) Fitbit® Inspire Activity Monitors (with instructions to share data with the dyad member and the study office); and 5) Instructions on how to create a secured account on the DUET website and instructions for logging on.
Arm Title
Delayed Intervention Group
Arm Type
Other
Arm Description
Participants assigned to the Delayed Intervention Group will receive a "Welcome Box" which on the outside is identical (and also is comparably weighted with bottled water) to that given to the Immediate Intervention group. This box would include: 1) Letters describing the project logistics and the important roles of each dyad member; and 2) monthly online study newsletters on topics unrelated to diet and exercise, but still of interest to cancer survivors and dyad members such as coping with stress, reducing exposure to radiation, sun safety, etc. to enhance retention and will be offered the opportunity to receive the online intervention after completing final 6-month assessments.
Intervention Type
Behavioral
Intervention Name(s)
eHealth Intervention
Intervention Description
Every week, each dyad member will receive a tailored text message that provides a new fun fact or that encourages them to log-on to the website to access findings of new research and how the results might apply to them. They will be directed to specific pages in the Web-based program and asked to select strategies from a list that they will practice during the upcoming week. Graphic displays of their progress will be provided along with SCT-based feedback. They will be directed to the website to record their behavioral goals for the upcoming week. Tips also will be provided for effective communication to enhance couple efficacy. All usage will be tracked to assess adherence.
Primary Outcome Measure Information:
Title
Body Weight
Description
Change in measured body weight
Time Frame
baseline
Title
Body Weight
Description
Change in measured body weight
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Waist Circumference
Description
measured with a non-stretch tape
Time Frame
baseline
Title
Waist Circumference
Description
measured with a non-stretch tape
Time Frame
6 months
Title
Physical Activity (self-reported)
Description
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Time Frame
Baseline
Title
Physical Activity (self-reported)
Description
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Time Frame
3 months
Title
Physical Activity (self-reported)
Description
Godin Leisure Time Physical Activity Questionnaire (4-item survey) - individuals provide the number of minutes of vigorous, moderate and light physical activity per week. The minimum is 0 - theoretically, the maximum is 10,080 (the number of minutes in a week), then they are asked if this level of activity is "typical." The higher the number of minutes of totaled moderate + vigorous activity, the better.
Time Frame
6 months
Title
Physical Activity (objective)
Description
Accelerometry (7-day assessment)
Time Frame
baseline
Title
Physical Activity (objective)
Description
Accelerometry (7-day assessment)
Time Frame
6 months
Title
Diet Quality
Description
Two 24-hour dietary recalls
Time Frame
baseline
Title
Diet Quality
Description
Two 24-hour dietary recalls
Time Frame
6 months
Title
Physical Performance (endurance)
Description
2-minute step test
Time Frame
Baseline
Title
Physical Performance (endurance)
Description
2-minute step test
Time Frame
6 months
Title
Physical Performance (lower body strength)
Description
30-second chair stand
Time Frame
Baseline
Title
Physical Performance (lower body strength)
Description
30-second chair stand
Time Frame
6 months
Title
Physical Performance (agility)
Description
8' foot up and go
Time Frame
Baseline
Title
Physical Performance (agility)
Description
8' foot up and go
Time Frame
6 months
Title
Physical Performance (gait speed)
Description
8' walk
Time Frame
baseline
Title
Physical Performance (gait speed)
Description
8' walk
Time Frame
6 months
Title
Physical Performance (Balance)
Description
Side-by-side, semi-tandem and tandem stances
Time Frame
baseline
Title
Physical Performance (Balance)
Description
Side-by-side, semi-tandem and tandem stances
Time Frame
6 months
Title
Self-efficacy for calorically restricted diet
Description
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Time Frame
baseline
Title
Self-efficacy for calorically restricted diet
Description
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Time Frame
3 months
Title
Self-efficacy for calorically restricted diet
Description
Clark et al. survey (20 items). Respondents either affirm or deny that they can resist high fat, high calorie foods under a variety of situations. Individuals who have maximum willpower achieve the top score of 20, whereas those with lesser willpower score lower (the minimum score is zero)
Time Frame
6 months
Title
Self-efficacy for increased physical activity
Description
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Time Frame
baseline
Title
Self-efficacy for increased physical activity
Description
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Time Frame
3 months
Title
Self-efficacy for increased physical activity
Description
Sallis et al. survey (6 items in total). Respondents rate themselves on each item from 0 to 100% on their level of confidence. The higher the total score (maximum of 100%) the better (Minimum 0%).
Time Frame
6 months
Title
Social support for calorically restricted diet
Description
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
baseline
Title
Social support for increased physical activity
Description
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
baseline
Title
Social support for calorically restricted diet
Description
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
3 months
Title
Social support for increased physical activity
Description
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
3 months
Title
Social support for calorically restricted diet
Description
Sallis et al. instrument (4 items). Respondents rate the level of support they obtain to follow a healthy, low calorie diet on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
6 months
Title
Social support for increased physical activity
Description
Sallis et al. instrument (4 items in total) Respondents rate the level of support they obtain to increase their level of physical activity on a 5-point scale ranging from ("never"= 0 to "everyday" = 4. Individuals who have maximum support achieve the top score of 16, whereas those with lesser support score lower (the minimum score is zero)
Time Frame
6 months
Title
Barriers for increased physical activity
Description
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Time Frame
baseline
Title
Barriers for increased physical activity
Description
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Time Frame
3 months
Title
Barriers for increased physical activity
Description
(15 items in total) Respondents either affirm or deny common barriers to exercise. Individuals who report more barriers achieve the top score of 21, whereas those with fewer barriers score lower (the minimum score is zero) and that is considered better.
Time Frame
6 months
Title
Circulating insulin
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating insulin
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating glucose
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating glucose
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating IL-6
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating IL-6
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating CRP
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating CRP
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating Total Cholesterol
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating Total Cholesterol
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating HDL Cholesterol
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating HDL Cholesterol
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating Tryglycerides
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating Tryglycerides
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating Adiponectin
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating Adiponectin
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Circulating Leptin
Description
assays on dried blood spot eluents
Time Frame
baseline
Title
Circulating Leptin
Description
assays on dried blood spot eluents
Time Frame
6 months
Title
Duke OARS Co-Morbidity Index
Description
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
Time Frame
baseline
Title
Duke OARS Co-Morbidity Index
Description
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
Time Frame
3 months
Title
Duke OARS Co-Morbidity Index
Description
43-item assessment of co-morbid conditions (multiple choice) (modified by removing 1 item)
Time Frame
6 months
Title
PROMIS v.1.2 GLOBAL HEALTH
Description
10-item Likert scale assessment of Quality of Life
Time Frame
Baseline
Title
PROMIS v.1.2 GLOBAL HEALTH
Description
10-item Likert scale assessment of Quality of Life
Time Frame
3 months
Title
PROMIS v.1.2 GLOBAL HEALTH
Description
10-item Likert scale assessment of Quality of Life
Time Frame
6 months
Title
EQ-5D-5L
Description
6-item Likert scale assessment of Quality of Life
Time Frame
Baseline
Title
EQ-5D-5L
Description
6-item Likert scale assessment of Quality of Life
Time Frame
3 months
Title
EQ-5D-5L
Description
6-item Likert scale assessment of Quality of Life
Time Frame
6 months
Title
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
Description
7-item scale to assess e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
Time Frame
Baseline
Title
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
Description
7-item scale to assess health and e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
Time Frame
3 months
Title
HEALTH / E-HEALTH LITERACY SCALE (NORMAN 2006)
Description
7-item scale to assess health and e-health literacy. Two items were added from eHEALS to understand consumer's interest in using eHealth in general.
Time Frame
6 months
Title
Barriers to Eating a Healthy Low Calorie Diet
Description
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
Time Frame
Baseline
Title
Barriers to Eating a Healthy Low Calorie Diet
Description
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
Time Frame
3 months
Title
Barriers to Eating a Healthy Low Calorie Diet
Description
(10 items) Respondents either affirm or deny common barriers to low calorie diet.
Time Frame
6 months
Title
PROMIS Emotional Distress: Depression - Short Form 8a
Description
(8 items) Likert scale assessment of depression
Time Frame
Baseline
Title
PROMIS Emotional Distress: Depression - Short Form 8a
Description
(8 items) Likert scale assessment of depression
Time Frame
3 months
Title
PROMIS Emotional Distress: Depression - Short Form 8a
Description
(8 items) Likert scale assessment of depression
Time Frame
6 months
Title
Smoking status
Description
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.
Time Frame
Baseline
Title
Smoking status
Description
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.
Time Frame
3 months
Title
Smoking status
Description
2 items that ask whether respondent has ever smoked >100 cigarettes and current smoking status.
Time Frame
6 months
Other Pre-specified Outcome Measures:
Title
Relationship to chosen partner
Description
1 item question that asks for relationship of chosen partner to cancer survivor
Time Frame
Baseline
Title
Socio-Demographic (George, et al, 1984)
Description
3-items that ask about income and perceptions of economic well-being
Time Frame
Baseline
Title
Socio-Demographic (George, et al, 1984)
Description
3-items that ask about income and perceptions of economic well-being
Time Frame
3 months
Title
Socio-Demographic (George, et al, 1984)
Description
3-items that ask about income and perceptions of economic well-being
Time Frame
6 months
Title
Circulating Insulin (TSH)
Description
assays on dried blood spot eluents
Time Frame
Baseline
Title
Circulating Insulin (TSH)
Description
assays on dried blood spot eluents
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults age 18+ for whom at least one dyad member has been diagnosed and completed curative treatment for localized renal cancer, or loco-regional ovarian, colorectal, endometrial, or female breast cancer. (Loco-regional prostate cancer survivors are also eligible but could be on active surveillance). Diagnosed as overweight or obese (BMI >25 kg/m2. Low vegetable and fruit intake (<2.5 cups day). Low physical activity (<150 minutes per week). English-speaking and writing. Completed at least 5th grade. Uses the internet and owns a mobile phone. Exclusion Criteria: Diagnosed with uncontrolled chronic conditions (i.e., diabetes, blood pressure, CVD, etc) Diagnosed with a health conditions that precludes adherence to an unsupervised weight loss intervention (e.g., pregnancy, end-stage renal disease, etc). Instructed by a physician to limit physical activity AND have paralysis, dementia, blindness, unstable angina, untreated stage 3 hypertension, or recent history of heart attack, congestive heart failure or pulmonary conditions that required oxygen or hospitalization within 6 months. Diagnosed with other cancers (except non-malignant skin cancer), cancer recurrence or metastatic disease. Resides in a skilled nursing or assisted living facility. Resides more than 15 minute driving distance from dyad partner.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendy Demark-Wahnefried, PhD, RD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
UAB School of Health Professions, Department of Nutrition Sciences
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan at the moment to share IDP.
Citations:
PubMed Identifier
34684474
Citation
Pekmezi DW, Crane TE, Oster RA, Rogers LQ, Hoenemeyer T, Farrell D, Cole WW, Wolin K, Badr H, Demark-Wahnefried W. Rationale and Methods for a Randomized Controlled Trial of a Dyadic, Web-Based, Weight Loss Intervention among Cancer Survivors and Partners: The DUET Study. Nutrients. 2021 Sep 29;13(10):3472. doi: 10.3390/nu13103472. Erratum In: Nutrients. 2022 Jul 29;14(15):
Results Reference
background

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