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Clinical Trials/NCT06335615
NCT06335615
Completed
N/A

Examining the Effectiveness, Mediators, and Moderators of a Brief Acceptance Intervention for Stress to Improve Students' Well-Being: A Randomized Controlled Trial

VU University of Amsterdam1 site in 1 country116 target enrollmentNovember 27, 2023
ConditionsStress

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stress
Sponsor
VU University of Amsterdam
Enrollment
116
Locations
1
Primary Endpoint
Psychological Well-Being
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The goal of this randomized controlled trial is to test a brief psychological intervention that focusses on acceptance of stress in a student population. The main questions it aims to answer are:

  • Does this brief acceptance intervention increase the well-being of students in the short term?
  • By which mechanisms does this effect occur?
  • What are moderating factors of this effect?

Half of the participants follow a one-hour intervention, which includes

  • psychoeducation and metaphors about stress and how acceptance can help to deal with it
  • experiential exercises
  • mindfulness meditation
  • mindfulness homework practice

Students that receive the intervention will be compared to students that merely received psychoeducation about stress and acceptance to see if the intervention lead to larger increases in well-being.

Registry
clinicaltrials.gov
Start Date
November 27, 2023
End Date
December 19, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
VU University of Amsterdam
Responsible Party
Principal Investigator
Principal Investigator

Jaap Lancee

Assistant Professor

VU University of Amsterdam

Eligibility Criteria

Inclusion Criteria

  • Student at the University of Amsterdam in the Bachelor's programme psychology or communication science

Exclusion Criteria

  • Panic Disorder as measured with the Rapid Measurement Toolkit-20 (Batterham et al., 2020; cutoff at 9)
  • Asthma, Chronic Obstructive Pulmonary Disease (COPD), another lung disease (including covid-related lung complaints), or tightness of chest
  • Pregnancy
  • Physical disability that limits ability to move and jump

Outcomes

Primary Outcomes

Psychological Well-Being

Time Frame: Change from baseline (1 - 14 days before the intervention/psychoeducation) to post measurement (3 days after the intervention/psychoeducation)

Psychological well-being was measured with the General Health Questionnaire-12 (GHQ-12, Goldberg \& Williams, 1988), which is a unidimensional measure of mental health with good psychometric properties (Romppel et al., 2013). Higher scores on the GHQ-12 indicate more psychological distress and lower well-being.

Secondary Outcomes

  • State Anxiety(Change from baseline (1 - 14 days before the intervention/psychoeducation) to post measurement (3 days after the intervention/psychoeducation))
  • Study Stress(Change from baseline (1 - 14 days before the intervention/psychoeducation) to post measurement (3 days after the intervention/psychoeducation))
  • Psychological Flexibility(Change from baseline (1 - 14 days before the intervention/psychoeducation) to post measurement (3 days after the intervention/psychoeducation))
  • Interoceptive awareness(Change from baseline (1 - 14 days before the intervention/psychoeducation) to post measurement (3 days after the intervention/psychoeducation))

Study Sites (1)

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