Skip to content

Delivery of Enhance Fitness Trial

Evaluation of Remotely Delivered Versus In-person Enhance Fitness for Arthritis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05275348
Acronym
DEFT
Enrollment
310
Registered
2022-03-11
Start date
2022-02-02
Completion date
2024-01-31
Last updated
2022-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthritis, Fibromyalgia, Gout, Lupus or SLE, Osteoarthritis, Rheumatoid Arthritis

Keywords

physical activity, arthritis, rural

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.

Interventions

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.

BEHAVIORALIn-person Enhance Fitness

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.

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
University of Washington
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion 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. 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.

Design outcomes

Primary

MeasureTime frameDescription
Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short form6 month follow upA 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

MeasureTime frameDescription
30-second Bicep Curl TestStudy months: 0, 4Standard physical test conducted by Enhance Fitness instructors of number of arm curls in 30 seconds
Timed Up and Go TestStudy months: 0, 4Standard physical test conducted by Enhance Fitness instructor of 8 foot timed up-and-go
DepressionStudy months: 0, 4, 10, 16PROMIS 29 Depression Short Form
UCLA 3-item Loneliness ScaleStudy months: 0, 4, 10, 163 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'.
FatigueStudy months: 0, 4, 10, 16PROMIS 29 Fatigue Short Form
Patient-Reported Outcome Measurement Information System (PROMIS) 10-item short formStudy months: 0, 4, 16A 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).
Pain InterferenceStudy months: 0, 4, 10, 16Measured by the PROMIS 29 Pain Interference Short Form
30-second Sit-to-Stand TestStudy months: 0, 4Standard physical test conducted by Enhance Fitness instructors of number of sit to stands in 30 seconds

Other

MeasureTime frameDescription
AnxietyStudy months: 0, 4, 10, 16PROMIS 29 Anxiety short form
Sleep DisturbanceStudy months: 0, 4, 10, 16PROMIS 29 Sleep disturbance short form
Ability to Participate in Social Roles and ActivitiesStudy months: 0, 4, 10, 16PROMIS 29 Ability to Participate in Social Roles and Activities short form
International Physical Activity Questionnaire- Short FormStudy months: 0, 4, 10, 16Self-reported time spent engaging in types and intensities of physical activity and sitting time.
Exercise Self-Efficacy ScaleStudy months: 0, 4, 10, 169 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.

Countries

United States

Contacts

Primary ContactElise Hoffman
evh3@uw.edu206-616-4671
Backup ContactLouisa Sopher
lsopher@uw.edu206-221-1765

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026