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Efficacy of the self-help intervention "This is your life"

Efficacy of the self-help intervention "This is your life": A randomized controlled trial to improve well-being and flourishing for adults with a low or moderate level of well-being

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23561
Enrollment
372
Registered
2013-11-29
Start date
2014-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Well-being, flourishing, resilience, positive psychology Welbevinden, floreren, veerkracht, positieve psychologie

Interventions

Study design: A randomized controlled trial with three conditions: 1. Experimental condition 1: the self-help intervention "This is your life, experience the effects of positive psychology" with wee

Sponsors

University of Twente
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Participant is between 18 and 65 years • Participant experiences a low or moderate level of well-being ("languishers" or "moderately mentally healthy") • Participant has sufficient internet connection and an e-mailadress • Participant is willing to invest an average time of 4 hours per week during 8-12 weeks when he or she is in one of the experimental conditions. • Participant masters the Dutch language to fill in questionnaires and follow the self-help intervention independently. • Participant gives informed consent for participating in the study.

Exclusion criteria

Exclusion criteria: Participants who are flourishing and thus have high levels of well-being: They score 1) high (4 or 5) on one or more items of the subscale "emotional well-being" of the Mental Health Continuum Short Form (MHC-SF), and 2) high (4 or 5) on six or more items of a combination of the subschales "social well-being" and "psychological wellbeing" of the MHC-SF. • Presence of serious depressive or anxiety symptoms: score of >10 on the depressionscale and/or score of >10 on the anxietyscale of the Hospital Anxiety and Depression Scale (HADS).

Design outcomes

Primary

MeasureTime frame
The primary outcome is the level of well-being, measured with the MHC-SF.

Secondary

MeasureTime frame
Secundary study parameters/outcome of the study (if applicable): Secondary outcomes are flourishing, mental illnesses (depression and anxiety), positive and negative emotions, resilience, use of strengths, optimism, self-compassion, positive relationships, health care use and productivity losses. Demographics, personality characteristics and positive and negative life events during the last 12 months will also be measured.

Contacts

Public ContactMarijke Schotanus-Dijkstra

University of Twente Postbus 217

m.schotanus@utwente.nl053-4893491

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)