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The Effectiveness of a Mindfulness Application on Perceived Stess

Erasmus University logo

Erasmus University

Status

Completed

Conditions

Burnout
Mindfulness
mHealth
Stress

Treatments

Other: Structured 8-week mHealth mindfulness program

Study type

Interventional

Funder types

Other

Identifiers

NCT05246800
METC 2017-1117

Details and patient eligibility

About

Mindfulness has become increasingly popular and positive outcomes have been reported for mindfulness-based interventions (MBIs) in reducing stress. The aim of this study is to investigate if a non-guided mindfulness mobile phone application can decrease perceived stress in a non-clinical Dutch population over the course of eight weeks, with follow-up at six months.

Full description

Background:

Mindfulness has become increasingly popular and positive outcomes have been reported for mindfulness-based interventions (MBIs) in reducing stress. These findings make room for innovative perspectives on how MBIs could be applied, for instance through mHealth.

Objectives:

The aim of this study is to investigate if a non-guided mindfulness mobile phone application can decrease perceived stress in a non-clinical Dutch population over the course of eight weeks, with follow-up at six months.

Methods:

A randomized controlled trial (RCT) was performed, comparing the experimental group that made use of a structured 8-week mHealth mindfulness program and a control group after 8 weeks, with follow-up after six months. Participants were recruited via a national television program. The primary outcome measure was perceived stress as measured by the Perceived Stress scale (PSS), secondary outcomes were symptoms of burnout (VAS) and psychological symptoms (measured by the four-dimensional symptom questionnaire ; 4DSQ at follow-up). Outcomes were analyzed using a multilevel regression model.

Enrollment

587 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

>18 years

Exclusion criteria

There were no other eligibility criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

587 participants in 2 patient groups

Experimental group
Experimental group
Description:
a structured 8-week mHealth mindfulness program.
Treatment:
Other: Structured 8-week mHealth mindfulness program
Control group
No Intervention group
Description:
The control group was suggested to read the information about stress and burnout on the website of the TV-programme.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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