NCT07714954

Brief Summary

Young adults who experience depression and/or anxiety symptoms (i.e., internalizing symptoms) will be randomly allocated 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.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
15mo left

Started Oct 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress5%
Oct 2026Feb 2028

First Submitted

Initial submission to the registry

June 23, 2026

Completed
27 days until next milestone

First Posted

Study publicly available on registry

July 20, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2028

Last Updated

August 14, 2026

Status Verified

May 1, 2026

Enrollment Period

1.3 years

First QC Date

June 23, 2026

Last Update Submit

August 11, 2026

Conditions

Keywords

meaning in lifemeaning-centered interventioninternalizing symptomsdepression symptomsanxiety symptoms

Outcome Measures

Primary Outcomes (2)

  • Depression Anxiety Stress Scale (DASS-21)

    self-report questionnaire: DASS-21: sum score (0-63), 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)

  • Meaning in Life Questionnaire (MLQ); presence of meaning subscale

    self-report questionnaire: MLQ: sum score (5-35), 7-point Likert scale (1-7), higher scores indicating higher presence of life meaning

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

Study Arms (2)

Meaning-centered intervention

EXPERIMENTAL

* Participants receive a meaning-centered intervention consisting of six 1-hour online sessions led by a trainer. * Interventions: Behavioral: Meaning-centered intervention for individuals who tend to feel down or anxious

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

Waitlist control

NO INTERVENTION

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

Interventions

* 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 the workbook * Homework assignments designed to deepen participants' experience and reflection on meaning in their daily lives

Also known as: Meaning-centered intervention for internalizing symptoms adapted from the intervention "Meaning-centered intervention for youth worrying about their weight and shape".
Meaning-centered intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • heightened internalizing symptoms (depression and/or anxiety symptoms) as indicated by PHQ-4 score of 2 or above on either the anxiety or depression subscale

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

DepressionAnxiety Disorders

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 23, 2026

First Posted

July 20, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

February 1, 2028

Study Completion (Estimated)

February 1, 2028

Last Updated

August 14, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share