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Pre-surgery pain class may ease joint replacement recovery

NCT ID NCT07362589

Symptom relief Sponsor: Yeditepe University Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 giving patients a pain education booklet and video before knee or hip replacement surgery helps them feel less anxious and have less pain afterward. About 70 adults scheduled for elective joint replacement will be randomly assigned to receive the education or usual care. Researchers will measure pain, anxiety, painkiller use, and hospital stay length.

What this could mean

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

Active substance
pain education booklet and video
What this could lead to
If it works, this simple education approach could help patients feel less anxious and experience less pain after joint replacement surgery.
What could go wrong
This is a small, early-stage study with only 70 participants, so results may not apply to everyone. The intervention is just education, so it may not meaningfully change pain or anxiety.

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

About 70 people

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

Started

Jul 2025

Expected to finish

Jan 2026

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

18 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: * Being 18 years of age or older, * Providing voluntary informed consent to participate in the study, * Scheduled to undergo elective knee or hip joint replacement (arthroplasty) surgery, * Having no communication barriers, * Having no history of alcohol or substance dependence, * Having no concurrent diagnosis of malignant disease and not receiving cancer treatment, * Not using opioid medications regularly in the preoperative period, * Having an ASA score of III or below, * Having no cognitive impairment that would affect the ability to comprehend the provided education, * Having no diagnosed neurological or psychiatric disorder and not using medications related to such conditions. Exclusion criteria: \- Patients who do not meet the specified inclusion criteria will not be included in the study. Elimination criteria: * Indication for postoperative intensive care, * Development of major complications after surgery, such as massive bleeding or pulmonary embolism, * Requesting to withdraw from the study at any stage, * Use of a patient-controlled analgesia device postoperatively

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Conditions

The condition(s) this trial relates to.

agnosia osteoarthritis Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Arthroplasty Hip replacement Knee replacement Pain management

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    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

  • Yeditepe Üniversitesi Hastanesi

    Istanbul, Kayişdaği, Turkey (Türkiye)

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