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Delivery of Enhance Fitness Trial (DEFT)

Primary Purpose

Arthritis, Rheumatoid Arthritis, Fibromyalgia

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tele-Enhance Fitness
In-person Enhance Fitness
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Arthritis focused on measuring physical activity, arthritis, rural

Eligibility Criteria

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

For participants 65 years or older

Inclusion Criteria:

  • CDC defined arthritis (answering yes to the following: "Have you EVER been told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia?")
  • Community-dwelling
  • English-speaking

Exclusion Criteria:

  • cognitive impairment (Mini Montreal Cognitive Assessment [Mini MoCA version 2.1] score <11)
  • significant, non-corrected visual or hearing impairment
  • pregnancy
  • physician does not recommend exercise due to a contraindicating health condition

For participants 18-64 years old:

  • CDC defined arthritis (answering yes to the following: "Have you EVER been told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia?")
  • Community-dwelling
  • English-speaking
  • One of the following additional criteria: (a) moderate-to-severe functional limitation, (b) low household income, or (c) living in a rural area. The definitions of these additional criteria are shown below.

    1. Functional limitation: Reporting some difficulty or limitation to doing any of the physical activities listed in the PROMIS 10-item Physical Function Short Form (e.g., bathing, dressing, shopping, walking) will be considered to have moderate to severe functional limitation.
    2. Low Income: Given that income and cost of living can vary geographically (e.g., urban vs. rural), the investigators will use the Department of Housing and Urban Development's low income limit that determines eligibility for various housing programs. Low income is 80 percent of the median income for a given household size and location based on the US Census Bureau's American Community Survey. Lookup tables are published online annually. These questions will be asked in the screening questionnaire by the UW Study Team who will then reference the correct lookup tables to check if participant meets the definition for low income.
    3. Rural Area: The investigators will apply the widely used National Center for Health Statistics urban-rural classification scheme to identify rural counties. The UW Study Team will ask potential participants the county that they currently live in during the telephone screening and will reference the National Center for Health Statistics urban-rural codes to check if the county is classified as rural.

Exclusion Criteria:

  • cognitive impairment (Mini Montreal Cognitive Assessment [Mini MoCA version 2.1] score <11)
  • significant, non-corrected visual or hearing impairment
  • pregnancy
  • physician does not recommend exercise due to a contraindicating health condition

Sites / Locations

  • University of WashingtonRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tele-EF

In-person EF

Arm Description

Remote delivery of Enhance Fitness.

In-person delivery of Enhance Fitness.

Outcomes

Primary Outcome Measures

Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short form
A 10-item questionnaire that assesses the participant's physical functioning (i.e., one's ability to perform activities that require physical action, such as self-care, walking indoors or outdoors, or climbing stairs).

Secondary Outcome Measures

Pain Interference
Measured by the PROMIS 29 Pain Interference Short Form
30-second Sit-to-Stand Test
Standard physical test conducted by Enhance Fitness instructors of number of sit to stands in 30 seconds
30-second Bicep Curl Test
Standard physical test conducted by Enhance Fitness instructors of number of arm curls in 30 seconds
Timed Up and Go Test
Standard physical test conducted by Enhance Fitness instructor of 8 foot timed up-and-go
Depression
PROMIS 29 Depression Short Form
UCLA 3-item Loneliness Scale
3 question questionnaire used to assess 3 dimensions of loneliness including relational connectedness, social connectedness and self-perceived isolation. Participants rate these domains from 1-3 (hardly ever, some of the time, or often) with a total score from 3-9 with a lower score indicating 'least lonely' and a higher score indicating 'most lonely'.
Fatigue
PROMIS 29 Fatigue Short Form
Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short form
A 10-item questionnaire that assesses the participant's physical functioning (i.e., one's ability to perform activities that require physical action, such as self-care, walking indoors or outdoors, or climbing stairs).

Full Information

First Posted
February 9, 2022
Last Updated
March 1, 2022
Sponsor
University of Washington
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT05275348
Brief Title
Delivery of Enhance Fitness Trial
Acronym
DEFT
Official Title
Evaluation of Remotely Delivered Versus In-person Enhance Fitness for Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 2, 2022 (Actual)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Arthritis is a common condition in the United States, and a leading cause of pain and disability. Physical exercise is recommended for managing arthritis, but access to evidence-based exercise programs is limited, particularly in rural areas. Therefore, the investigators propose to evaluate remote delivery of an evidence-based exercise program called Enhance Fitness (EF) that is recommended for arthritis management. The primary purpose of this study is to determine if remotely delivered EF is non-inferior to in-person EF on primary and secondary outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthritis, Rheumatoid Arthritis, Fibromyalgia, Gout, Osteoarthritis, Lupus or SLE
Keywords
physical activity, arthritis, rural

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
310 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tele-EF
Arm Type
Experimental
Arm Description
Remote delivery of Enhance Fitness.
Arm Title
In-person EF
Arm Type
Active Comparator
Arm Description
In-person delivery of Enhance Fitness.
Intervention Type
Behavioral
Intervention Name(s)
Tele-Enhance Fitness
Intervention Description
Tele-Enhance Fitness (tele-EF) is a community-based exercise program for older adults. It is a supervised group exercise program that will meet virtually 3 times a week for 1 hour for 4 months. Each tele-EF class uses a standardized format that includes a 5-minute warm-up phase, 25 minutes of moderate-intensity aerobic conditioning, 20 minutes of progressive strength training, and 10 minutes of cool down involving flexibility and balance exercises. Strength training involves progressive resistance exercises, using adjustable 1- to 10-pound ankle and wrist weights. Tele-EF classes will be led by an instructor trained in administering EF through a virtual format. EF instructors will be able to monitor and correct participant's movements through videoconference. All tele-EF classes are monitored by a "spotter" who watches participants exercise using gallery mode.
Intervention Type
Behavioral
Intervention Name(s)
In-person Enhance Fitness
Intervention Description
Enhance Fitness is a community-based exercise program for older adults. It is a supervised group exercise program that will meet in person 3 times a week for 1 hour for 4 months. Each EF class uses a standardized format that includes a 5-minute warm-up phase, 25 minutes of moderate-intensity aerobic conditioning/walking, 20 minutes of progressive strength training, and 10 minutes of cool down involving flexibility and balance exercises. Strength training involves progressive resistance exercises, using adjustable 1- to 10-pound ankle and wrist weights. Classes will be led by an instructor trained in administering Enhance Fitness.
Primary Outcome Measure Information:
Title
Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short form
Description
A 10-item questionnaire that assesses the participant's physical functioning (i.e., one's ability to perform activities that require physical action, such as self-care, walking indoors or outdoors, or climbing stairs).
Time Frame
6 month follow up
Secondary Outcome Measure Information:
Title
Pain Interference
Description
Measured by the PROMIS 29 Pain Interference Short Form
Time Frame
Study months: 0, 4, 10, 16
Title
30-second Sit-to-Stand Test
Description
Standard physical test conducted by Enhance Fitness instructors of number of sit to stands in 30 seconds
Time Frame
Study months: 0, 4
Title
30-second Bicep Curl Test
Description
Standard physical test conducted by Enhance Fitness instructors of number of arm curls in 30 seconds
Time Frame
Study months: 0, 4
Title
Timed Up and Go Test
Description
Standard physical test conducted by Enhance Fitness instructor of 8 foot timed up-and-go
Time Frame
Study months: 0, 4
Title
Depression
Description
PROMIS 29 Depression Short Form
Time Frame
Study months: 0, 4, 10, 16
Title
UCLA 3-item Loneliness Scale
Description
3 question questionnaire used to assess 3 dimensions of loneliness including relational connectedness, social connectedness and self-perceived isolation. Participants rate these domains from 1-3 (hardly ever, some of the time, or often) with a total score from 3-9 with a lower score indicating 'least lonely' and a higher score indicating 'most lonely'.
Time Frame
Study months: 0, 4, 10, 16
Title
Fatigue
Description
PROMIS 29 Fatigue Short Form
Time Frame
Study months: 0, 4, 10, 16
Title
Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short form
Description
A 10-item questionnaire that assesses the participant's physical functioning (i.e., one's ability to perform activities that require physical action, such as self-care, walking indoors or outdoors, or climbing stairs).
Time Frame
Study months: 0, 4, 16
Other Pre-specified Outcome Measures:
Title
International Physical Activity Questionnaire- Short Form
Description
Self-reported time spent engaging in types and intensities of physical activity and sitting time.
Time Frame
Study months: 0, 4, 10, 16
Title
Exercise Self-Efficacy Scale
Description
9 item 0 to 10 scale used to assess participant's confidence in their ability to exercise when presented with obstacles. Total scores range from 0-90 with higher scores indicating higher exercise self-efficacy.
Time Frame
Study months: 0, 4, 10, 16
Title
Anxiety
Description
PROMIS 29 Anxiety short form
Time Frame
Study months: 0, 4, 10, 16
Title
Sleep Disturbance
Description
PROMIS 29 Sleep disturbance short form
Time Frame
Study months: 0, 4, 10, 16
Title
Ability to Participate in Social Roles and Activities
Description
PROMIS 29 Ability to Participate in Social Roles and Activities short form
Time Frame
Study months: 0, 4, 10, 16

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
For participants 65 years or older Inclusion Criteria: CDC defined arthritis (answering yes to the following: "Have you EVER been told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia?") Community-dwelling English-speaking Exclusion Criteria: cognitive impairment (Mini Montreal Cognitive Assessment [Mini MoCA version 2.1] score <11) significant, non-corrected visual or hearing impairment pregnancy physician does not recommend exercise due to a contraindicating health condition For participants 18-64 years old: CDC defined arthritis (answering yes to the following: "Have you EVER been told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia?") Community-dwelling English-speaking One of the following additional criteria: (a) moderate-to-severe functional limitation, (b) low household income, or (c) living in a rural area. The definitions of these additional criteria are shown below. Functional limitation: Reporting some difficulty or limitation to doing any of the physical activities listed in the PROMIS 10-item Physical Function Short Form (e.g., bathing, dressing, shopping, walking) will be considered to have moderate to severe functional limitation. Low Income: Given that income and cost of living can vary geographically (e.g., urban vs. rural), the investigators will use the Department of Housing and Urban Development's low income limit that determines eligibility for various housing programs. Low income is 80 percent of the median income for a given household size and location based on the US Census Bureau's American Community Survey. Lookup tables are published online annually. These questions will be asked in the screening questionnaire by the UW Study Team who will then reference the correct lookup tables to check if participant meets the definition for low income. Rural Area: The investigators will apply the widely used National Center for Health Statistics urban-rural classification scheme to identify rural counties. The UW Study Team will ask potential participants the county that they currently live in during the telephone screening and will reference the National Center for Health Statistics urban-rural codes to check if the county is classified as rural. Exclusion Criteria: cognitive impairment (Mini Montreal Cognitive Assessment [Mini MoCA version 2.1] score <11) significant, non-corrected visual or hearing impairment pregnancy physician does not recommend exercise due to a contraindicating health condition
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Elise Hoffman
Phone
206-616-4671
Email
evh3@uw.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Louisa Sopher
Phone
206-221-1765
Email
lsopher@uw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kushang V Patel, PhD, MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elise Hoffman
Phone
206-616-4671
Email
evh3@uw.edu

12. IPD Sharing Statement

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Delivery of Enhance Fitness Trial

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