Shiatsu shows promise for fatigue in arthritis study
NCT ID NCT05433168
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether shiatsu, a type of bodywork using finger pressure, can reduce fatigue in people with axial spondyloarthritis (a form of arthritis affecting the spine). 72 adults with the condition were randomly assigned to receive shiatsu sessions or continue usual care, then switched groups. The main goal was to see if shiatsu improved fatigue scores on a standard questionnaire. The study is complete, but results are not yet reported.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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72 people
The number who actually took part.
- Started
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Sep 2022
- Finished
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Dec 2024
- Lead sponsor
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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
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * The patients with spondyloarthritis meeting the ASAS criteria and followed in the rheumatology department of the Orléans Regional Hospital Center. * Men and women aged 18 to 70 * Patients with digital or visual analog rating scale ≥ 3 on the 1st question of the BASDAI Exclusion Criteria: * Patient with a pathology that contraindicates the practice of shiatsu (evolving infectious skin pathology that would make shiatsu treatment difficult) * Previous shiatsu treatment * Inability to attend appointments for the duration of the study * Pregnant or breastfeeding woman * Refusal to participate in the study or to sign the consent * Patients not affiliated or not beneficiaries of a social security scheme * Person under guardianship or curatorship * Patient with an uncontrolled epileptic or psychotic condition which, in the opinion of the investigator, would interfere with the smooth running of the study
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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
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CHU Orléans
Orléans, 45067, France
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Other studies related to the condition(s) this trial covers.
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