Clinical trial Recruiting at 1 site Interventional Ages 18 to 60

Everyday movement and subjective energy (MASE Project)

Official title: The Motor Activity - Subjective Energy (MASE) Project: Neurobiological and Digital Phenotyping Towards Digital Mental Health Interventions in Depression

Run by University of Bern · NCT07059234 · Data updated 2026-11-12

This project tests whether increasing everyday, non-exercise activity can boost feelings of energy and reduce depressive symptoms in people with major depressive disorder or recent remission.

Quick facts

Study typeInterventional
Ages18 Years to 60 Years
SexAll
Enrollment180 (estimated)
SponsorUniversity of Bern
Academic / other
Locations1 site (Bern)
StatusRecruiting
StartedSeptember 2, 2025
Main results expectedApril 30, 2027
Study endsApril 30, 2027
Registry record updatedSeptember 16, 2025
Trial IDNCT07059234 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults who speak German and either have current major depressive disorder (MADRS > 15) or remission within the past year with MADRS < 10 for at least one month, and who can wear activity monitors and complete electronic diaries, are ideal candidates.

Probably not a fit

People with other psychiatric disorders, acute suicidality, incompatible medical implants, pregnancy at baseline, or those unable to complete the monitoring procedures are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The MASE project uses wrist-worn accelerometers and electronic momentary diaries to link non-exercise activity (NEA) with real-time reports of subjective energy in daily life. Researchers will identify each person's activity–energy association (ASEA) and combine those data with neural markers to guide personalized behavioral activation that targets incidental movement. The intervention focuses on small, rewarding everyday actions (not structured exercise) to increase NEA and subjective energy, with outcomes including changes in depressive symptoms and relapse risk. Control and comparison groups, including remitted patients and healthy volunteers, are used to differentiate disorder-specific patterns.

Why it matters

Potential benefit: If successful, this approach could increase daily energy and lower depressive symptoms by tailoring behavioral activation to boost incidental physical activity.

How similar studies have gone: Previous work shows behavioral activation helps MDD and that incidental everyday activity is linked to higher subjective energy, but interventions explicitly targeting personalized NEA associations are still novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Sufficient knowledge of the German language
* Written informed consent.
* Score \> 15 on the Montgomery Asberg Depression rating scale (MADRS) for MDD group.
* Remission within the past year and exhibit a MADRS score \< 10 for at least one month for rMDD group

Exclusion Criteria:

* Pregnancy at baseline
* Claustrophobia
* Pacemaker
* Artificial heart valves
* Active implants
* Other psychiatric disorders
* Acute suicidality, change of medication / psychotherapy during the intervention (not dosage but substance).
* For healthy participants: history of any mental health condition or first-degree relative with affective / psychotic disorder

Where it's running

  • University of Bern
    Bern, Switzerland
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.