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Completed

NCT Number: NCT02041741

Improving Happiness in Flanders

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Psychology and Educational Sciences

Leuven, 3000, Belgium

About this study

This randomized trial has two aims:

  • 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.
  • 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:
  • a condition in which daily small and concrete happiness tips are sent to participants during one month via email (n=400)
  • 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)
  • 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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • no fluency in Flemish
  • living outside of Flanders

Treatment and study plan

Weekly tips

Behavioral

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

Daily Tips

Behavioral

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

Primary outcomes

  1. Subjective Happiness Scale

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

  2. Steen Happiness Inventory

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

Secondary outcomes

  1. Positive and Negative Affect Scale (PANAS)

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

  2. Patient Health Questionnaire-9 (PHQ-9)

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

  3. Warwick Edinburgh Mental Well-Being Scale

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

  4. Brief Symptom Inventory (KKL, Korte KlachtenLijst)

    Time frame: 4 weeks after start of intervention and 6 months after end of intervention

Other outcomes

  1. Meaning in Life Questionnaire

    Time frame: Start of intervention (predictor variable)

  2. Depressive Experiences Questionnaire (DEQ)

    Time frame: Start of intervention (predictor variable)

  3. Experiences in Close Relationships-Revised (ECR-R)

    Time frame: Start of intervention (predictor variable)

  4. Kentucky Inventory of Mindfulness (KIMS)

    Time frame: Start of intervention (predictor variable)

  5. Toronto Alexithymia Scale (TAS)

    Time frame: Start of intervention (predictor variable)

Sponsors and collaborators

Lead sponsor

Universitaire Ziekenhuizen KU Leuven

Other

Registry information

Official study title

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

Acronym: HAP-FLA

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jan 22, 2014
Registry last updated
May 29, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.