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Knee surgery prep: could coaching ease your nerves?

NCT ID NCT05217420

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Aug 04, 2026 · Updated 3 times

Summary

This study tests a behavioral program called Moving Well to see if it can reduce anxiety and depression in people waiting for knee replacement surgery. About 79 participants will either get the coaching program or a general wellness program. The goal is to improve emotional well-being before and after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Moving Well behavioral coaching program
What this could lead to
If it works, this could provide a simple, drug-free way to reduce anxiety and depression before knee replacement surgery.
What could go wrong
This is a small, early-stage study with only 79 participants. The results may not apply to everyone, and the program may not significantly improve mood.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

101 people

The number who actually took part.

Started

Apr 2022

Finished

Jan 2025

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

50 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: * Subjects must have their primary TKR (one knee or both knees) scheduled in 8 weeks or more * Be willing to participate in the Moving Well (intervention) arm or Staying Well (attention control) arm * Are willing to work with a coach * ≥ 50 years of age * Speak English * Have access to the internet, computer, and a working phone * We will prioritize the recruitment of subjects with low socioeconomic status defined as being a beneficiary of Medicaid or no insurance and an underrepresented racial/ethnic group (Hispanic/Black). Exclusion Criteria: * Non-English speakers * The intervention will first be delivered in English to ensure feasibility with the content before adapting the material for patients who speak other languages. * TKR was a result of a septic joint or revision (implant malfunction) * Unable to exercise (e.g., bed bound or wheelchair bound) * Have had contralateral TKR or other joint replacement surgery (hip, shoulder) within the past 5 years * If they have RA or other connective tissue disease: Lupus, ankylosing spondylitis, psoriatic arthritis, scleroderma, infectious arthritis, polymyalgia rheumatica.

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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.

Contacts and locations

Locations

  • Weill Cornell Medicine Clinical & Translational Science Center

    New York, New York, 10065, United States

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