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

NCT ID: NCT05289544

Last Updated: 2024-10-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

267 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-04-01

Study Completion Date

2024-09-10

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Arthritis Gout Fibromyalgia Rheumatoid Arthritis Osteoarthritis Lupus Erythematosus, Systemic

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Phone-Based Walk With Ease Program

Telephone-based Walk With Ease Program adapted from the Arthritis Foundations program

Group Type EXPERIMENTAL

Phone-Based Walk With Ease

Intervention Type BEHAVIORAL

6 week phone-delivered Walk With Ease Program

Delayed Phone-Based Walk With Ease Program

Telephone-Based Walk With Ease Program starting after the 1 year assessment

Group Type OTHER

Phone-Based Walk With Ease

Intervention Type BEHAVIORAL

6 week phone-delivered Walk With Ease Program

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Phone-Based Walk With Ease

6 week phone-delivered Walk With Ease Program

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of South Carolina

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Christine A Pellegrini, PhD

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of South Carolina

Columbia, South Carolina, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Pro00115106

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Fitness and Exercise for People With Arthritis
NCT00252070 COMPLETED PHASE2/PHASE3
The Osteoarthritis Prevention Study
NCT05946044 RECRUITING NA