CClinicalTrials.gg
CompletedNCT07058181Updated Mar 4, 2026

Meaning-centered Intervention for Internalizing Symptoms

An interventional study of Meaning-centered intervention for individuals who tend to feel down or anxious in Depressive and/or Anxiety Symptoms, sponsored by University of Groningen. Completed at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-04.

Sponsored by University of Groningen · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Nov 2024, registered May 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
155
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Young adults with internalizing symptoms will be randomly assigned to a six-session meaning-centered intervention condition or a waitlist condition. Both conditions receive the same questionnaires at baseline, post assessment (intervention condition: immediately after the final session; waitlist: four weeks after baseline), and follow-up.

The researchers hypothesize that a meaning-centered intervention for individuals with internalizing symptoms will increase participants' meaning in life and reduce their internalizing symptoms at post assessment and 4-week follow-up when compared to a waitlist condition.

Read the detailed description

First-year psychology students at the University of Groningen will be screened for depressive and anxiety symptoms. Those with heightened symptoms will be invited via e-mail to participate in the study. After filling out the baseline assessment online, participants will be randomly assigned to either a meaning-centered intervention condition, which will receive a meaning-centered intervention taking place approximately every four days, or a waitlist condition, which will be assigned no task. Participants in the intervention condition will follow six 1-hour online intervention sessions led by a trainer and conduct intervention-related homework assignments. The sessions can be followed in English, Dutch, or German. The intervention aims to increase participants' meaning in life and reduce their internalizing symptoms (i.e. depressive and/or anxiety symptoms). Immediately after the final session (i.e. approximately one month after the baseline assessment), participants in the intervention condition will be asked to fill in the post assessment, which includes the same questionnaires as the baseline assessment. Participants in the waitlist control will be asked to complete the post assessment one month after their baseline assessment. One month after the post assessment, participants in both conditions are asked to fill in same set of questionnaires. Waitlist participants are offered to receive the intervention sessions after the study has finished. Participants are compensated with SONA credits.

02

Conditions studied

  • Depressive and/or Anxiety Symptoms

Keywords

  • meaning-centered intervention
  • internalizing symptoms
  • young adults
03

In context

Lead sponsor

University of Groningen is the lead sponsor of 22 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • heightened internalizing symptoms (depressive and/or anxiety symptoms) as indicated by PHQ-4 total score of 2 or higher

Exclusion criteria

Exclusion Criteria:

  • receiving psychotherapeutic treatment for a depressive or anxiety disorder
  • suicidality
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
155 participants (actual)

Study arms

  • Experimental
    Meaning-centered intervention

    Participants receive a meaning-centered intervention consisting of six 1-hour online sessions led by a trainer.

    Behavioral: Meaning-centered intervention for individuals who tend to feel down or anxious

  • No intervention
    Waitlist control

    No task or intervention is assigned to participants in this arm.

Interventions

  • BehavioralMeaning-centered intervention for individuals who tend to feel down or anxious

    Meaning-centered intervention for internalizing symptoms adapted from the intervention "Meaning-centered intervention for youth worrying about their weight and shape". * Six 1-hour individual online sessions, approximately every 4 days * Sessions led by a certified trainer based on intervention manual * Four sources of meaning will be explored: personal life story, dealing with life's limitations, creating one's own life, and meaningful experiences * Participants follow intervention using intervention workbook * Homework assignments designed to deepen participants' experience and reflection on meaning in their daily lives

06

What researchers measure

Primary outcomes

  1. Meaning in Life Questionnaire; Depression, Anxiety and Stress Scales-21

    questionnaire (MLQ: sum score (5-35), 7-point Likert scale (1-7), higher scores indicating higher presence of life meaning; DASS-21: sum score (0-33), 4-point Likert scale (0-3), higher scores indicating higher internalizing symptoms)

    Time frame: at baseline; post (one month after baseline); one-month follow-up (one month after post)

Secondary outcomes

  1. Dyscontrolled drinking; Three-dimensional meaning

    questionnaire (Dyscontrolled drinking: sum score (3-27), 9-point Likert scale (1-9), higher scores indicating higher dyscontrolled drinking; Three-dimensional meaning: sum score (11-77), 7-Point Likert scale (1-7), higher scores indicating higher life meaning)

    Time frame: at baseline; post (one month after baseline); one-month follow-up (one month after post)

07

Study locations

1 site
  • Heymans Institute
    Groningen, Provincie Groningen 9712 TS, Netherlands
08

References and documents

Study documents

  • Protocol, analysis plan and consent form · Jun 19, 2025

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07058181
Lead sponsor
University of Groningen
Collaborators
University of Amsterdam
Responsible party
Marcel Näther (principal investigator, University of Groningen) — Principal investigator
First posted
Jul 10, 2025
Start date
Nov 28, 2024
Primary completion
Feb 23, 2026
Completion
Feb 23, 2026
Last update
Mar 4, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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