Phone-based program aims to get seniors moving and reduce arthritis pain
NCT ID NCT06623669
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a 6-month mobile program can help 200 older adults (65+) with knee or hip arthritis pain become more active, lose weight, and feel less pain. Participants will join weekly group or individual coaching calls and track their steps. After the program, they will try to keep up the healthy habits on their own for another 12 months. The goal is to see if this approach improves daily steps, pain, and physical function better than usual care.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Aug 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 65+ years * Body mass index of 30-45 kg/m2 or \>45 kg/m2 with physician's approval * No loss or gain of more than 5% body mass in previous 6 months * Presence of knee or hip osteoarthritis as ascertained via the Roux questionnaire * Independently living * Low active (i.e., not participating in regular resistance training and/or \>20 mins/day of aerobic exercise on more than 2 days/week in past 3 months as ascertained via a modified CHAMPS questionnaire) * Have no contraindication for safe and optimal participation in exercise based on EASY screening (pertaining to chest pain and discomfort during physical activity, dizziness or light headedness, or frequent falls and use of assistive devices) * Not currently using a weight loss medication (medications for diabetes management are permitted if weight stable) * Approved for participation by medical director * Willing to provide informed consent and agree to all study procedures and assessments. Exclusion Criteria: * Reside in skilled nursing facility, rehab or assisted living environment * History of pharmacologic treatment for a psychiatric disorder other than depression/anxiety within past year * Current untreated and/or unstable clinical depression or anxiety (Patient Health Questionnaire (PHQ-9) \>15) * Hospitalization for psychiatric event within past year prior to screening * History of mild cognitive impairment or dementia * Cognitive impairment (\<32) on Modified Telephone Interview for Cognitive Status survey (TICS-M) * Hearing or visual impairment that would preclude use of the videoconferencing software * Severe arthritis or other musculoskeletal disorder that is a contraindication for safe walking * Presently undergoing treatment for orthopedic fracture * Currently using a weight loss medication (medications for diabetes management are permitted if weight stable) * Contraindication based on EASY screening (pertaining to chest pain and discomfort during physical activity, dizziness or light headedness, or frequent falls and use of assistive devices) without physician approval * Joint replacement or other orthopedic surgery in past 6 months * Joint replacement or other orthopedic surgery planned in next 18 months * Have a diagnosis of uncontrolled hypertension; current or recent past (within 1 year) severe symptomatic heart disease, uncontrolled angina, stroke, chronic respiratory disease other than asthma or COPD, any disease requiring oxygen use, neurological or hematological disease; cancer requiring current treatment, except non-melanoma skin cancers; kidney failure requiring dialysis; have a Katz ADL disability; or engage in heavy alcohol use \>14 drinks/week. * Current participation in other research study with a prospective intervention * Unable/unwilling to commit to study protocol, including random assignment and use of technology tools * Unable/unwilling to attend three virtual testing appointments
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Wake Forest University
RECRUITINGWinston-Salem, North Carolina, 27109, United States
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