Skip to main content
Clinical Trials/NCT05060393
NCT05060393
Unknown
Not Applicable

Efficacy of Mindfulness-based Mobile Application Use in Patients With Depressive Disorder

University of Basel1 site in 1 country140 target enrollmentMay 1, 2021
ConditionsDepression

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
University of Basel
Enrollment
140
Locations
1
Primary Endpoint
Change from baseline self reported Depression Severity
Last Updated
4 years ago

Overview

Brief Summary

The presented randomized-controled study aim to assess the use of internet-based mindfulness intervention via mobile application for 30 days in patients with Major Depressive Disorder (MDD)

Detailed Description

Mindfulness-based interventions (MBI) proved to be effective in relapse prevention in MDD. Next, MBI in form of free mobile applications can be an effective augmentation of the treatment as usual (TAU) and can fill a gap in the ambulatory care. Given this background, the aim of this randomized controlled study is to assess the effectiveness of additional MBI via mobile app on the symptom severity and stress levels, compared to TAU.

Registry
clinicaltrials.gov
Start Date
May 1, 2021
End Date
January 1, 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jan Sarlon

Principal Investigator

University of Basel

Eligibility Criteria

Inclusion Criteria

  • Depression, current ill

Exclusion Criteria

  • acute alcohol- and drug dependency, schizophrenia or psychotic disorder, severe somatic illnes, not having smartphone or not willing to use mobile application

Outcomes

Primary Outcomes

Change from baseline self reported Depression Severity

Time Frame: 30 days

Beck Depression Inventory

Change from Baseline Depression Severity

Time Frame: 30 days

Hamilton Depression Rating Scale

Secondary Outcomes

  • Change from baseline tobacco consumption(30 days)
  • Change from baseline heart rate(30 days)
  • Change in consumption of anxiolytics(30 days)
  • Change from baseline alcohol consumption(30 days)
  • Change from baseline blood pressure(30 days)
  • Change from baseline respiratory rate(30 days)

Study Sites (1)

Loading locations...

Similar Trials