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Health and Energy Through Active Living Every Day After Cancer Intervention for Cancer Survivors (HEALED)

Primary Purpose

Quality of Life, Cognitive Decline, Fatigue

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Physical activity experiment
Balance and flexibility control
Sponsored by
American Cancer Society, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Quality of Life focused on measuring cancer, physical activity, sedentary behavior

Eligibility Criteria

55 Years - 77 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Are a survivor of Stage I - III breast, colon, endometrium, kidney, or bladder cancer, or of multiple myeloma (verified through medical record abstraction/tumor tissue or state registry, to which participants have already consented)
  • Are a part of the CPS-3 Portal (this also implies that an email address is on file and an English survey response)
  • Must have a physical, continental US street address where they can receive shipments for 12 months.
  • Have access to a working smartphone or tablet
  • Are not currently pregnant
  • Exercise less 300 minutes per week
  • Did not register for HEALED Study pilot (n = 99; conducted in 2019, published in 2021; Appendix 11, AM12_IRB00059007 approved in February 2019)
  • Are able to walk assisted

Exclusion Criteria:

  • A doctor has recommended that they avoid moderate or vigorous exercise, or limit walking
  • Have received any of the following treatments for their cancer diagnosis in the last 6 months: Surgery to remove the cancer, chemotherapy, radiation therapy, or immunotherapy.
  • Have major planned surgery in the next 12 months

Sites / Locations

  • American Cancer Society (virtual recruitment and study)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Physical Activity Group

Balance and Flexibility Group

Arm Description

Physical activity (PA) group participants will receive behavioral nudge e-mails with links to a web-based platform which will provide: physical activity information, at-home exercise demonstrations/videos for survivors of all fitness levels, articles, blog posts, physical activity/sitting recommendations, a space for goal setting, a platform for physical activity tracking, a discussion board, automatic syncing of their Fitbit to the leaderboard, etc.

The static Balance and Flexibility (BF) website will include infographics, videos, and articles for participants to view at their leisure. They will receive access to the HEALED website at the end of the 12-month intervention period.

Outcomes

Primary Outcome Measures

Sedentary time
Device-measured sedentary time with research-grade accelerometer
Physical activity
Device-measured light, moderate, vigorous intensity physical activity with research-grade accelerometer and Fitbit.

Secondary Outcome Measures

PROMIS Sleep Disturbance
5-item questionnaire measuring self-reported alertness, sleepiness, tiredness, and functional impairments associated with sleep problems during waking hours within the past seven days.
CPS-3 Fatigue Questions
A 5-item Likert scale measuring fatigue, lack of energy and general tiredness within the past month.
PROMIS Global Mental and Physical Health
Instrument consists of ten global health items that represent five core PROMIS domains (physical function, pain, fatigue, emotional distress, social health). Four items are used to assess global physical health. Four items are used to assess global mental health, all of which are administered using five-category response scales. Higher scores indicate better mental/physical health.
Emotional Distress-Anxiety
A PROMIS assessment of 8-items on the pure domain of anxiety in individuals age 18 and older. High scores indicate higher anxiety symptom severity.
Emotional Distress-Depression
A PROMIS assessment of 7-items on the pure domain of depression in individuals age 18 and older. High scores indicate higher depression symptom severity.
PROMIS Cognitive Function
This item bank assesses patient-perceived cognitive deficits. Facets include mental acuity, concentration, verbal and nonverbal memory, verbal fluency, and perceived changes in cognitive functions. Higher scores indicate higher cognitive funciton.
30 second sit-stand test
Video-administered, self-reported sit-stand test (validity study: https://pubmed.ncbi.nlm.nih.gov/34797895/)

Full Information

First Posted
April 27, 2022
Last Updated
February 2, 2023
Sponsor
American Cancer Society, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05356988
Brief Title
Health and Energy Through Active Living Every Day After Cancer Intervention for Cancer Survivors
Acronym
HEALED
Official Title
Health and Energy Through Active Living Every Day After Cancer Intervention for Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
July 24, 2023 (Anticipated)
Study Completion Date
August 24, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
American Cancer Society, Inc.

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 the Health and Energy through Active Living Every Day (HEALED) intervention, is to examine the effect of a web-based intervention on changes in device-measured physical activity (light and moderate-to-vigorous intensity aerobic) and sedentary behavior. The purpose of this study is intended for survivors of a cancer with a 5-year survival (at Stage I, II, and III) of at least 45% that has a strong level of evidence for association with physical inactivity according to the 2018 PA Guidelines Advisory Committee Report (breast, colon, endometrium, kidney, bladder, multiple myeloma). In line with social cognitive theory behavior change techniques, participants will be provided information and skills necessary to be more physically active and less sedentary after a cancer diagnosis. New materials will be disseminated biweekly through a website open only to participants, and include at-home exercise demonstration videos, research news, discussion boards, success stories, infographics for exercise recommendations, etc.
Detailed Description
By 2026, there will be approximately 20.3 million cancer survivors in the U.S., and this population is expected to grow with improved cancer survival rates. Cancer survivors experience a myriad of side effects following treatment, including fatigue, decreased muscle mass, balance issues, decreased cognitive function, and an increased risk of comorbidities. Observational studies and randomized controlled trials suggest that physical activity (PA) is a safe and effective non-pharmacologic option for improving some of these side effects. Despite the evidence, it is estimated that at least 75% of cancer survivors do not meet PA guidelines. Interventions tailored for survivors may increase PA, but there are gaps in the literature regarding the most effective methods. Further, there are several cancers associated with physical inactivity, but most PA interventions focus on breast cancer. Additionally, many existing interventions require in-person meetings, are very resource-intensive, and may not be sustainable. Most physical activity interventions focus on the promotion of moderate-vigorous PA, ignoring the importance of decreased sedentary time and increased light PA. Accordingly, it is imperative to create more sustainable, broad-reaching PA and sedentary behavior interventions that are intended for survivors of various physical inactivity-associated cancers. The proposed one-year study will be a two-arm, randomized control intervention embedded within the Cancer Prevention Study-3 (CPS-3), a prospective cohort study of cancer incidence and mortality initiated by the American Cancer Society. The proposed Health and Energy through Active Living Every Day (HEALED) intervention is intended for survivors of a cancer with an expected 5-year survival (at Stage I, II or III) of at least 45% that has a strong level of evidence for association with physical inactivity according to the 2018 PA Guidelines Advisory Committee Report (breast, colon, endometrium, kidney, multiple myeloma, and bladder). In line with social cognitive theory behavior change techniques, participants will be provided information and skills necessary to be more physically active and less sedentary after a cancer diagnosis. Materials and tools will be updated monthly through a secure website open only to participants, and include: at-home exercise demonstration videos, steps leaderboards, goal setting tools, Fitbit self-monitoring and syncing capabilities, discussion boards, success stories, infographics for exercise recommendations, etc. This intervention will add to the very minimal evidence base for PA interventions for diverse cancer survivors in a sustainable, broad-reaching manner. Further, the data resulting from this study will provide insight towards promotion of the "time-use" approach, which focuses on all of the movement behaviors (including sedentary time, light intensity physical activity, and moderate-to-vigorous physical activity), which has not yet been used in interventions for survivors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Quality of Life, Cognitive Decline, Fatigue, Sleep, Anxiety, Depression
Keywords
cancer, physical activity, sedentary behavior

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The intervention group will have access for one year to a website to help increase aerobic and strength training activities. The control group will have access for one year to a website to help improve balance and flexibility. At the end of the one-year study, each group will get access to the opposite website.
Masking
None (Open Label)
Masking Description
Investigator will not be involved in randomization, but given the obvious differences in treatment vs. control, participants, investigator, and assessors will be aware of assignment.
Allocation
Randomized
Enrollment
415 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Physical Activity Group
Arm Type
Experimental
Arm Description
Physical activity (PA) group participants will receive behavioral nudge e-mails with links to a web-based platform which will provide: physical activity information, at-home exercise demonstrations/videos for survivors of all fitness levels, articles, blog posts, physical activity/sitting recommendations, a space for goal setting, a platform for physical activity tracking, a discussion board, automatic syncing of their Fitbit to the leaderboard, etc.
Arm Title
Balance and Flexibility Group
Arm Type
Active Comparator
Arm Description
The static Balance and Flexibility (BF) website will include infographics, videos, and articles for participants to view at their leisure. They will receive access to the HEALED website at the end of the 12-month intervention period.
Intervention Type
Behavioral
Intervention Name(s)
Physical activity experiment
Intervention Description
The Physical Activity (PA) group will have access for one year to the PA website to help increase aerobic and strength training activities.
Intervention Type
Behavioral
Intervention Name(s)
Balance and flexibility control
Intervention Description
The static Balance and Flexibility (BF) website will include infographics, videos, and articles for participants to view at their leisure around stretching and balance exercises.
Primary Outcome Measure Information:
Title
Sedentary time
Description
Device-measured sedentary time with research-grade accelerometer
Time Frame
12 months
Title
Physical activity
Description
Device-measured light, moderate, vigorous intensity physical activity with research-grade accelerometer and Fitbit.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
PROMIS Sleep Disturbance
Description
5-item questionnaire measuring self-reported alertness, sleepiness, tiredness, and functional impairments associated with sleep problems during waking hours within the past seven days.
Time Frame
12 months
Title
CPS-3 Fatigue Questions
Description
A 5-item Likert scale measuring fatigue, lack of energy and general tiredness within the past month.
Time Frame
12 months
Title
PROMIS Global Mental and Physical Health
Description
Instrument consists of ten global health items that represent five core PROMIS domains (physical function, pain, fatigue, emotional distress, social health). Four items are used to assess global physical health. Four items are used to assess global mental health, all of which are administered using five-category response scales. Higher scores indicate better mental/physical health.
Time Frame
12 months
Title
Emotional Distress-Anxiety
Description
A PROMIS assessment of 8-items on the pure domain of anxiety in individuals age 18 and older. High scores indicate higher anxiety symptom severity.
Time Frame
12 months
Title
Emotional Distress-Depression
Description
A PROMIS assessment of 7-items on the pure domain of depression in individuals age 18 and older. High scores indicate higher depression symptom severity.
Time Frame
12 months
Title
PROMIS Cognitive Function
Description
This item bank assesses patient-perceived cognitive deficits. Facets include mental acuity, concentration, verbal and nonverbal memory, verbal fluency, and perceived changes in cognitive functions. Higher scores indicate higher cognitive funciton.
Time Frame
12 months
Title
30 second sit-stand test
Description
Video-administered, self-reported sit-stand test (validity study: https://pubmed.ncbi.nlm.nih.gov/34797895/)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
77 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Are a survivor of Stage I - III breast, colon, endometrium, kidney, or bladder cancer, or of multiple myeloma (verified through medical record abstraction/tumor tissue or state registry, to which participants have already consented) Are a part of the CPS-3 Portal (this also implies that an email address is on file and an English survey response) Must have a physical, continental US street address where they can receive shipments for 12 months. Have access to a working smartphone or tablet Are not currently pregnant Exercise less 300 minutes per week Did not register for HEALED Study pilot (n = 99; conducted in 2019, published in 2021; Appendix 11, AM12_IRB00059007 approved in February 2019) Are able to walk assisted Exclusion Criteria: A doctor has recommended that they avoid moderate or vigorous exercise, or limit walking Have received any of the following treatments for their cancer diagnosis in the last 6 months: Surgery to remove the cancer, chemotherapy, radiation therapy, or immunotherapy. Have major planned surgery in the next 12 months
Facility Information:
Facility Name
American Cancer Society (virtual recruitment and study)
City
Kennesaw
State/Province
Georgia
ZIP/Postal Code
30144
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33954891
Citation
Rees-Punia E, Leach CR, Westmaas JL, Dempsey LF, Roberts AM, Nocera JR, Patel AV. Pilot Randomized Controlled Trial of Feasibility, Acceptability, and Preliminary Efficacy of a Web-Based Physical Activity and Sedentary Time Intervention for Survivors of Physical Inactivity-Related Cancers. Int J Behav Med. 2022 Apr;29(2):220-229. doi: 10.1007/s12529-021-09999-5. Epub 2021 May 6. Erratum In: Int J Behav Med. 2023 Apr;30(2):304.
Results Reference
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Health and Energy Through Active Living Every Day After Cancer Intervention for Cancer Survivors

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