NCT07433764

Brief Summary

This study aims to establish the test-retest reliability of the WB6Dim digital self-assessment tool across its eight well-being dimensions, using a 3-day interval protocol designed to minimize the probability of genuine well-being changes between assessments. Participants complete the 28-item WB6Dim questionnaire at baseline (T1) and again 3 days later (T2). A single contamination control question at T2 identifies participants who experienced a significant life event during the interval; these pairs are excluded from primary ICC analyses and retained for exploratory analyses. An optional third assessment at 9 weeks (T3) provides preliminary exploratory data on sensitivity to change following access to a well-being program. T3 is not part of the primary design.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
0mo left

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress98%
Feb 2026May 2026

First Submitted

Initial submission to the registry

February 19, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

February 19, 2026

Completed
3 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 22, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 25, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 9, 2026

Expected
Last Updated

February 25, 2026

Status Verified

February 1, 2026

Enrollment Period

3 days

First QC Date

February 19, 2026

Last Update Submit

February 19, 2026

Conditions

Keywords

well-beingTest-retest reliabilityIntraclass correlationDigital self-assessmentWB6DimPsychometric validationWorkplace well-being

Outcome Measures

Primary Outcomes (8)

  • Test-Retest Reliability (ICC) of the WB6Dim Internal Tension Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Sleep and Recovery Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Energy Reservoir Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Self-Esteem Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Emotional Climate Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Cognitive Saturation Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Hyperconnection Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1.Higher values indicate greater temporal stability.

    Day 0 to Day 3

  • Test-Retest Reliability (ICC) of the WB6Dim Perceived Autonomy Dimension

    ICC(1,1) on contamination-free T1/T2 pairs. Score range: 0 to 1. Higher values indicate greater temporal stability.

    Day 0 to Day 3

Secondary Outcomes (2)

  • Contamination Rate at T2

    Day 3

  • ICC Comparison Between Contamination-Free and Contaminated Pairs

    Day 0 to Day 3

Other Outcomes (8)

  • Exploratory Sensitivity to Change - Sleep and Recovery

    Day 0 to Week 9

  • Exploratory Sensitivity to Change - Internal Tension

    Day 0 to Week 9

  • Exploratory Sensitivity to Change - Energy Reservoir

    Day 0 to Week 9

  • +5 more other outcomes

Study Arms (1)

Cohort C - Test-Retest Reliability

Adult volunteers recruited from a health and well-being newsletter subscriber base. Participants complete the 28-item WB6Dim digital self-assessment at baseline (T1) and again 3 days later (T2). A contamination control question at T2 identifies participants who experienced a significant life event during the interval. An optional third assessment (T3) is completed at 9 weeks by participants who voluntarily accessed a well-being program after T2 completion.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult volunteers recruited from a French health and well-being newsletter subscriber base. Not selected based on medical conditions. Represents the general adult population with an interest in personal well-being and health prevention.

You may qualify if:

  • Adults aged 18 years or older
  • Able to read and understand French
  • Access to an internet-connected device
  • Willing to complete the WB6Dim questionnaire at T1 and T2
  • Consent to anonymous data collection for research purposes

You may not qualify if:

  • Under 18 years of age
  • Unable to read or understand French

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Clover Link

Bandol, 83150, France

RECRUITING

Related Publications (1)

  • Alitta Q. Validation Study of the WB6Dim Digital Self-Assessment Tool for Well-Being Using Gold-Standard Psychometric Scales. ClinicalTrials.gov NCT07301879. First posted 2025-12-24.

    BACKGROUND

Related Links

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Frédérique MD, PhD RETORNAZ, MD, PhD

    European Hospital, Unit of Care and Research in Internal Medicine and Infectious Diseases.

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
9 Weeks
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 19, 2026

First Posted

February 25, 2026

Study Start

February 19, 2026

Primary Completion

February 22, 2026

Study Completion (Estimated)

May 9, 2026

Last Updated

February 25, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

13:12All collected data are fully anonymized at the point of entry. No individual-level identifiable data are stored or processed. Participant email addresses are used solely for matching T1 and T2 responses and are not retained after study completion. All analyses are conducted on aggregated, pseudonymized numerical data only. IPD sharing is therefore not applicable.

Locations