Can a Step-by-Step activity program help people recover from burnout?
NCT ID NCT07407829
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a psychologist-guided physical activity program, based on CBT and ACT, can be used in regular care for adults with stress-related exhaustion. About 12 to 20 participants will take part in 5 to 6 sessions, logging activity and completing questionnaires. The goal is to see if the program is feasible, safe, and acceptable, not yet to prove it works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CBT/ACT-based psychologist-delivered physical activity program
- What this could lead to
- If this program works, it could offer a practical way to help people with stress-related exhaustion build healthy physical activity habits as part of their regular care.
- What could go wrong
- This is a very small feasibility study with only 20 participants, so results may not apply to everyone. It is designed to test if the program can be delivered, not yet to prove it improves symptoms.
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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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- 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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20 to 64 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.
Show the full entry requirements Hide 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 * Adult aged 20 to 64 years. * Experiencing stress-related exhaustion, assessed in regular clinical care (for example, symptoms consistent with exhaustion disorder or a closely related stress-related condition). * Symptoms are not in the acute phase (participant is able to engage in outpatient psychological treatment and gradual physical activity). * Elevated fatigue/exhaustion at screening, indicated by scores on screening questionnaires (Karolinska Exhaustion Disorder Scale and Multidimensional Fatigue Inventory). * Able to understand spoken and written Swedish. * Has access to a smartphone, tablet, or computer with an internet connection to complete study questionnaires and activity logging. * No medical condition that makes physical activity unsafe, based on clinical screening and participant self-report. Exclusion Criteria * Currently receiving psychological treatment outside the recruiting clinic that is expected to interfere with participation in the program or study assessments. * Current or past diagnosis of a psychotic disorder. * Current or past diagnosis of bipolar disorder. * Severe mental health condition requiring another primary treatment approach at this time (for example, severe major depressive disorder, post-traumatic stress disorder, or an eating disorder). * Ongoing substance use disorder. * Medical condition or acute illness that makes physical activity inappropriate at this time (for example, recent blood clot, severe infection, or other serious condition). * Severe musculoskeletal condition that substantially limits ability to perform physical activity. * Started antidepressant medication within the past 4 weeks. Additional notes (not eligibility criteria): Participants may use psychotropic medication (for example, antidepressants, sleep medication, or anxiety medication) if the medication regimen is stable. Participants will be asked to report any medication changes during the study period. Mild to moderate comorbid anxiety or depression is allowed if stress-related exhaustion is the primary clinical problem.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Avonova Occupational Health
RECRUITINGStockholm, Sweden
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