Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
Healthy Volunteers
NCT07059234

The Motor Activity - Subjective Energy (MASE) Project

Led by University of Bern · Updated on 2025-09-16

180

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

Sponsors

U

University of Bern

Lead Sponsor

U

University of Salzburg

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

The Motor Activity - Subjective Energy (MASE) Project

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Bern

Bern, Switzerland, 3012

Actively Recruiting

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Research Team

C

Claudio R. Nigg, Prof

CONTACT

L

Lea Nitzpon, M.Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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