ClinicalTrials.Veeva

Menu

Improving Happiness in Flanders (HAP-FLA)

U

Universitaire Ziekenhuizen KU Leuven

Status

Completed

Conditions

Happiness in the General Population

Treatments

Behavioral: Weekly tips
Behavioral: Daily Tips

Study type

Interventional

Funder types

Other

Identifiers

NCT02041741
HAP-FLA

Details and patient eligibility

About

This study aims to assess the effects of two different types of interventions aimed at increasing happiness in the Flemish general population as compared to individuals that receive no intervention.

Full description

This randomized trial has two aims:

  1. First, it investigates the efficacy of two different happiness interventions in increasing feelings of happiness in the Flemish general population using a wait-list controlled design.
  2. Second, this study aims to identify predictors of response in both interventions ("what works for whom?")

Methods

Design and procedure

  • Participants will be contacted through social media and directed to a website that is specifically designed for this study.

  • All participants who register for the study first will electronically sign an informed consent and will be asked to complete a brief battery of questionnaires online (base line measures) before randomization.

  • Participants then are assigned randomly using a block-randomized design to one of the three conditions using a computerized algorithm:

    1. a condition in which daily small and concrete happiness tips are sent to participants during one month via email (n=400)
    2. a condition in which weekly more in-depth happiness tips with a (doing and experiencing) task are given during one month via email (n=400)
    3. a wait-list condition (1 month); these participants will be subsequently (after the end of the 4-week intervention) randomized to condition (a) or (b) (n=400) using a block-randomized design.
  • All participants will be assessed weekly during the intervention (see below) and followed-up 6 months after the end of the study.

Measures

Participants will complete a detailed demographic questionnaire.

Primary outcome measures:

  • Subjective Happiness Scale (SHS; Lyubomirsky & Lepper, 1999)
  • Steen Happiness Inventory (SHI; Seligman, Steen, Park, & Peterson, 2005)

Secondary outcome measures

  • Positive and Negative Affect Scales (PANAS; Watson, Clark, & Tellegen, 1988)
  • Patient Health Questionnaire-9 (PHQ-9; Kroenke, Spitzer, & Williams, 2001)
  • Warwick Edinburgh Mental Well-Being Scale (WEMWBS; Tennant et al., 2007)
  • Brief Symptom Inventory (Korte KlachtenLijst; KKL; Lange, & Appelo, 2007)

Predictors of outcome

  • Meaning in Life Questionnaire (MLQ; Steger, Frazier, Oishi, & Kaler, 2006)
  • Depressive Experiences Questionnaire (DEQ; Blatt, D'Afflitti, & Quinlan, 1976)
  • Experiences in Close Relationships-Revised (ECR-R, Fraley, Waller, & Brennan, 2000)
  • Kentucky Inventory of Mindfulness (KIMS; Baer, Smith, & Allen, 2004)
  • Toronto Alexithymia Scale (TAS; Bagby, Parker, & Taylor, 1994)

Data analyses

Repeated measures Anova and multilevel modeling will be used to assess differences between the three conditions in primary and secondary outcomes at the end of the intervention and at follow-up. Regression analyses and growth curve modeling will be used to examine the effects of the predictors on primary and secondary outcomes.

Enrollment

10,863 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Sufficient fluency in Flemish
  • at least 18 years of age

Exclusion criteria

  • no fluency in Flemish
  • living outside of Flanders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

10,863 participants in 3 patient groups

Weekly tips
Active Comparator group
Description:
Daily small and concrete happiness tips
Treatment:
Behavioral: Weekly tips
Daily Tips
Active Comparator group
Description:
Weekly more in-depth happiness tips involving an active (doing and experiencing) task
Treatment:
Behavioral: Daily Tips
Wait-List Control
No Intervention group
Description:
No intervention

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems