Phone-Based Based Walk With Ease Program for Adults With Arthritis

  • STATUS
    Recruiting
  • End date
    Sep 29, 2024
  • participants needed
    300
  • sponsor
    University of South Carolina
Updated on 23 April 2022
arthritis
lupus
rheumatoid arthritis
Accepts healthy volunteers

Summary

The objective of this study is to examine the short-term (6-weeks and 6 months) and long-term (1 year) effects of a phone-based version of Walk With Ease intervention.

Description

Participants will be randomized to either start the 6-week program immediately or after one year. Our Walk with Ease by Telephone (WWE-T) program is adapted from the original 6-week community-based group walking program developed by the Arthritis Foundation for adults with arthritis. The phone-based program will include 2 phone calls each week with a trained Walk With Ease Leader for 6 weeks. Assessments will be completed before at the start of the study, 6 weeks, 6 months and at 12 months.

Details
Condition Arthritis, Gout, Fibromyalgia, Rheumatoid Arthritis, Osteoarthritis, Lupus Erythematosus, Systemic
Treatment Phone-Based Walk With Ease
Clinical Study IdentifierNCT05289544
SponsorUniversity of South Carolina
Last Modified on23 April 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

told by a doctor or other health professional that you have some form of arthritis, rheumatoid arthritis, gout, lupus, fibromyalgia
able to read and write in English
plan to live in the Columbia, SC region for next year
willing to be randomized to either group
complete all baseline measure

Exclusion Criteria

contraindications to exercise (besides arthritis)
are pregnant, breastfeeding, or planning to become pregnant in the next year
have a serious cognitive impairment
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How to participate?

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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