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New program aims to ease chronic pain without pills

NCT ID NCT07273084

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This pilot study tested a 6-week group program for adults with chronic non-cancer pain. The program combined pain education, personalized exercises, and healthy lifestyle tips. Researchers measured quality of life, pain levels, and other factors in 12 participants before, after, and 3 months later. The goal was to see if this approach could help people manage pain better without relying on medication.

What this could mean

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

Active substance
Multidisciplinary intervention program (pain education, exercise, healthy habits)
What this could lead to
If it works, this could point toward a practical, non-drug approach to help people manage chronic pain and improve their daily life.
What could go wrong
This is a very small pilot study with only 12 people and no control group, so results may not be reliable or apply to others. The program is also short-term, so any benefits might not last.

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

12 people

The number who actually took part.

Started

Jul 2025

Finished

Feb 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

18 to 79 years

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: * Individuals aged between 18 and 79 years. * Individuals diagnosed with non-cancer chronic pain lasting more than 3 months. Exclusion Criteria: * Individuals with pain of oncologic origin. * Individuals who have experienced a fracture or undergone surgery within the past year. * Pregnant women. * Individuals without adequate understanding of the Spanish language. * Individuals with cognitive impairment that prevents them from performing the program's interventions. * Individuals with physical performance deficits that prevent them from carrying out the program's activities. * Individuals with urinary and/or fecal incontinence.

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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

  • Benicassim Health Center

    Benicassim, Castellón, 12560, Spain

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