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Phone-based program aims to get seniors moving and reduce arthritis pain

NCT ID NCT06623669

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2025

Expected to finish

Aug 2029

An estimate. End dates often move.

Lead sponsor

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

65 years and older

Sex

Anyone

Healthy volunteers

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

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.

Chronic Pain chronic pain syndrome Motor Activity Obesity obesity disorder osteoarthritis osteoarthritis, hip osteoarthritis, knee Overweight Sedentary Behavior Weight Loss

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Wake Forest University

    RECRUITING

    Winston-Salem, North Carolina, 27109, United States

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