Could a simple exercise program rewire emotional control in depression?
NCT ID NCT07780695
First seen Aug 21, 2026 · Last updated Aug 25, 2026 · Updated 2 times
Summary
This trial tests whether a structured, adapted physical activity program can improve emotion regulation in adults with depressive disorders who have recently been discharged from psychiatric hospitalization. Participants are randomly assigned to either a standard exercise program or one that also includes activities specifically targeting emotional regulation. The study measures changes in emotion regulation strategies, as well as depressive symptoms, anxiety, and self-esteem, to see if exercise offers a valuable complement to usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Adapted physical activity program (standard or combined with emotion-regulation activities)
- What this could lead to
- If effective, this could point toward a non-drug approach to help people with depression better manage their emotions after hospitalization.
- What could go wrong
- This is a small, early-stage trial, so results may not be conclusive or widely applicable. The program requires physical effort, which may be challenging for some participants.
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
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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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45 people
The number who actually took part.
- Started
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Feb 2023
- Finished
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Apr 2026
- 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 years and older
- 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: * Age over 18 years * Unipolar or bipolar depressive disorder * Discharged from full hospitalization, up to three weeks after discharge * Able to provide free and informed consent * Not participating in any other research Exclusion Criteria: * High suicidal risk, at the investigator's discretion * Medical contraindication to any physical activity * Motor, psychological, or intellectual disability, or other medical condition, at the investigator's discretion, preventing full participation in the study * Severe addictive disorder impeding participation in the study * Psychotic disorder * Pregnancy or breastfeeding * Any circumstances rendering the participant unable to understand the nature, purpose, or consequences of the trial * Under legal protection (guardianship or trusteeship) * No social security coverage
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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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EPSM de Vendée - Centre Hospitalier Georges Mazurelle
La Roche-sur-Yon, Vendée, 85 000, France
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