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Mind over MRI: could rewording scan reports ease back pain?

NCT ID NCT06103474

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jul 30, 2026 · Updated 2 times

Summary

This completed study tested whether changing the language in MRI reports can reduce the nocebo effect—where negative words in medical reports can make people feel worse. Researchers studied 18 adults with lower back pain who were getting an MRI. They compared standard reports to specially worded clinical reports to see if the new wording could improve pain scores and reduce anxiety.

What this could mean

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

What this could lead to
If successful, this could show that simple changes in how doctors write MRI reports can reduce pain and anxiety in patients with lower back pain.
What could go wrong
This is a very small, early study with only 18 participants, so results may not apply to everyone. The effect may be small or not reproducible.

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

18 people

The number who actually took part.

Started

Jan 2024

Finished

Nov 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

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: * History of lower back pain undergoing MRI * Greater than 18 years of age * Able to understand and willing to comply with all study procedures and is available for the duration of the study Exclusion Criteria: * A potential subject who meets any of the following criteria will be excluded from participation in the study: * Acute lower back pain secondary to trauma within 1 months * Severe cord compression on MRI * Cord signal abnormality on MRI * Metastatic cancer * Spinal epidural abscess * Vertebral osteomyelitis * Judgement of the ordering physician (e.g. focal neurologic deficit) * Anything that, in the opinion of the investigator or team, would place the subject at increased risk or preclude the subject's full compliance with or completion of the study

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As listed by the trial registrant

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

Contacts and locations

Locations

  • UAB

    Birmingham, Alabama, 35294, United States

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