Ireland
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Recruiting Not applicable

The Motor Activity - Subjective Energy (MASE) Project

NCT07059234 · tracked via the Priya Life Science Switzerland tracker
Phase
Not applicable
Started
2025-09-02
Last updated
2025-09-16

Condition(s) studied

Depressive Disorder, Major

Investigational drug(s) / intervention(s)

Non-exercise activity

Non-exercise activity: The 5-week intervention to assess the effects of non-exercise activity on the activity-subjective energy association incorporates two high-intensity Ambulatory Assessment (AA) weeks at the beginning and end, with a tapered 3-week Ecological Momentary Intervention (EMI) phase in between. Momentary targeted micro interventions (JITAIs) with a Within-Person-Encouragement Design (WPED) are used to tailor the activity to the individual situation and phenotype of each participant.

Study summary

This approach utilizes accelerometry to measure NEA and electronic diaries for real-time psychological assessments, overcoming limitations of traditional methods such as retrospective bias and low ecological validity. Brief episodes of physical activity in daily life, which are distinctly different from structured exercise sessions, are generally linked to improved affective well-being. Notably, feelings of energy are particularly associated with incidental, unstructured, and non-exercise activities. Clinically, psychomotor retardation and diminished mood are key diagnostic features of MDD, with evidence suggesting that lower motor activity differentiates MDD patients from controls and that increased activity correlates with treatment response. In this context, the MASE project aims to design personalized BA interventions that focus on increasing NEA and, in turn, enhancing subjective energy levels to reduce depressive symptoms and prevent relapse.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
Accepted
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

Primary outcome measure(s)

  • Change of real-life physical activity-subjective energy association — pre-post intervention (at 5 weeks)
    Subjective energy following target contexts will be assessed using the subscale Energetic Arousal from the MDMQ (VAS; scale from 0 to 100, with higher scores indicating higher energy levels).

Trial sites (1)

FacilityCityRegionStatus
University of Bern Bern Switzerland Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07059234 on ClinicalTrials.gov ↗ ← All trials in Switzerland