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Improving Happiness in Flanders

Happiness in Flanders: A Randomized, Wait-List Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02041741
Acronym
HAP-FLA
Enrollment
10863
Registered
2014-01-22
Start date
2014-01-31
Completion date
2014-10-31
Last updated
2015-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Happiness in the General Population

Keywords

happiness, well-being, distress, positive psychology

Brief summary

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.

Detailed 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.

Interventions

BEHAVIORALWeekly tips

Participants in this condition receive weekly a more in-depth tip to increase feelings of happiness involving a (doing and experiencing) task

BEHAVIORALDaily Tips

Participants in this condition receive daily a set of small tips aimed at increasing happiness

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

* no fluency in Flemish * living outside of Flanders

Design outcomes

Primary

MeasureTime frame
Subjective Happiness Scale4 weeks after start of intervention and 6 months after end of intervention
Steen Happiness Inventory4 weeks after start of intervention and 6 months after end of intervention

Secondary

MeasureTime frame
Positive and Negative Affect Scale (PANAS)4 weeks after start of intervention and 6 months after end of intervention
Patient Health Questionnaire-9 (PHQ-9)4 weeks after start of intervention and 6 months after end of intervention
Warwick Edinburgh Mental Well-Being Scale4 weeks after start of intervention and 6 months after end of intervention
Brief Symptom Inventory (KKL, Korte KlachtenLijst)4 weeks after start of intervention and 6 months after end of intervention

Other

MeasureTime frame
Depressive Experiences Questionnaire (DEQ)Start of intervention (predictor variable)
Experiences in Close Relationships-Revised (ECR-R)Start of intervention (predictor variable)
Kentucky Inventory of Mindfulness (KIMS)Start of intervention (predictor variable)
Toronto Alexithymia Scale (TAS)Start of intervention (predictor variable)
Meaning in Life QuestionnaireStart of intervention (predictor variable)

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026