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Personalized exercise coaching for fibromyalgia: a tiny trial that never got off the ground

NCT ID NCT03895086

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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 aimed to see if a personalized physical activity program, with one face-to-face session followed by phone coaching, could improve quality of life for people with fibromyalgia compared to standard group exercise classes. The trial was terminated after enrolling only one participant, so no meaningful results were obtained. The approach remains untested.

What this could mean

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

Active substance
physical activity program
What this could lead to
If it had succeeded, it could have pointed toward a more effective way to manage fibromyalgia symptoms through personalized exercise coaching.
What could go wrong
The trial was terminated after enrolling only one person, so no reliable conclusions can be drawn. The approach may not work for everyone or may be too difficult to implement widely.

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

1 person

The number who actually took part.

Started

Feb 2020

Finished

Jan 2021

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: * Major patient * Patient whose FIQ ≤ 59/100 * Patient who can be followed for 12 months in the CETD * Patient able to follow the adaptated physical activities proposed by "Siel Bleu", on the physical and organizational level * Patient with a smartphone and/or a computer (mac/pc) with an internet connection allowing the use of a tracking application linked to the activity tracker * Patient with the ability to understand protocol and consenting to participate in this study * Patient benefiting from a social cover Exclusion Criteria: * Patient participating in an interventional trial within 3 months of enrollment * Pregnant or lactating woman, or having the possibility to procreate without effective contraception * Patient minor, under guardianship, curators or deprived of liberty * Patient unable to follow the protocol, according to the judgment of the investigator, or refusing to use of digital applications * Patient with contraindications to physical activity * Patient having already followed the physical activities proposed by 'Siel Bleu"

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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

  • Centre Hospitalier Départemental Vendée

    La Roche-sur-Yon, France

  • Centre Hospitalier Universitaire

    Nantes, France

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