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Brain training vs. pain pills: new study aimed to ease Post-Surgery shoulder pain

NCT ID NCT05948007

Symptom relief Sponsor: Chang Gung Memorial Hospital 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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 planned to compare two approaches for managing pain after shoulder surgery: neurofeedback training (a technique that teaches you to control your brain activity) and a standard pain management program. The goal was to see which method better reduces pain, improves shoulder function, and boosts thinking skills. However, the study was withdrawn before enrolling any participants, so no results are available.

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.

Expected to start

Nov 2023

An estimate. Start dates often move.

Finished

May 2026

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * Pain ≥3months and ≥3 days per week * Pain intensity ≥ 40 (VAS scale from 0 no pain to 100 very painful) * Participants in the neurofeedback training group and pain management group were asked not to involve other treatment when they are in the 6th-12th week intervention period. * The surgical indication would be based on orthopedics opinions. Exclusion Criteria: * shoulder surgery in the prior 3 years * osteoporotic vertebral fractures or rheumatologic diseases * chronic wide- spread pain syndromes (fibromyalgia or chronic fatigue syndrome) * pain at any other location in addition to shoulder pain * Neurological disease, i.e., stroke, parkinson's disease, etc.. * Cancer

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Conditions

The condition(s) this trial relates to.

agnosia Pain, Postoperative Shoulder Pain

As listed by the trial registrant

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

Pain, shoulder Post operative pain

More trials for these conditions

Other studies related to the condition(s) this trial covers.