Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
285 participants
INTERVENTIONAL
2025-03-28
2029-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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45 minutes/week
Participants will be given a goal of 45 minutes/week of moderate-to-vigorous intensity physical activity
DREAM Adaptive Intervention
6-month physical activity program (Dose Response of Exercise for Arthritis Management (DREAM)) which includes monthly phone coaching, Walk With Ease Guidebook, behavioral lessons, and a Fitbit. Participants may receive additional contact (email, text, or phone) if they struggle to meet activity goal.
90 minutes/week
Participants will be given a goal of 90 minutes/week of moderate-to-vigorous intensity physical activity
DREAM Adaptive Intervention
6-month physical activity program (Dose Response of Exercise for Arthritis Management (DREAM)) which includes monthly phone coaching, Walk With Ease Guidebook, behavioral lessons, and a Fitbit. Participants may receive additional contact (email, text, or phone) if they struggle to meet activity goal.
150 minutes/week
Participants will be given a goal of 150 minutes/week of moderate-to-vigorous intensity physical activity
DREAM Adaptive Intervention
6-month physical activity program (Dose Response of Exercise for Arthritis Management (DREAM)) which includes monthly phone coaching, Walk With Ease Guidebook, behavioral lessons, and a Fitbit. Participants may receive additional contact (email, text, or phone) if they struggle to meet activity goal.
Interventions
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DREAM Adaptive Intervention
6-month physical activity program (Dose Response of Exercise for Arthritis Management (DREAM)) which includes monthly phone coaching, Walk With Ease Guidebook, behavioral lessons, and a Fitbit. Participants may receive additional contact (email, text, or phone) if they struggle to meet activity goal.
Eligibility Criteria
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Inclusion Criteria
* Have a doctor diagnosed form of arthritis, rheumatoid arthritis, gout, lupus, or fibromyalgia
* Ability to read and write in English
Exclusion Criteria
* Engage in ≥30 min/week of Actigraph assessed MVPA
* Are pregnant, breastfeeding, or planning to become pregnant in the next year
* Are planning to relocate out of the Columbia, SC area in the next 12 months,
* Do not have a device compatible with Fitbit
* Have uncontrolled hypertension (e.g., systolic blood pressure \> 160 mmHg or diastolic blood pressure \> 100 mmHg)
* Plan to have a surgery that affects mobility in the next 12 months
* Have a serious cognitive impairment.
* Not willing to be randomized to any of the 3 conditions, do not believe they could adhere to the goals, or do not believe they could achieve the highest dose of activity (150 minutes/week).
18 Years
ALL
No
Sponsors
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Centers for Disease Control and Prevention
FED
University of South Carolina
OTHER
Responsible Party
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Christine A Pellegrini, PhD
Associate Professor
Principal Investigators
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Christine Pellegrini, PhD
Role: PRINCIPAL_INVESTIGATOR
University of South Carolina
Locations
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University of South Carolina
Columbia, South Carolina, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Pro00140006
Identifier Type: -
Identifier Source: org_study_id
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