The Effectiveness of a Positive Psychology App in the General Population

Sponsor
University of Twente (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05292560
Collaborator
(none)
306
1
2
5.9
51.7

Study Details

Study Description

Brief Summary

The corona crisis has a negative impact on the mental wellbeing of the Dutch population. Positive psychology exercises (PPOs) can potentially improve mental well-being and reduce mild and moderate psychological complaints. Previous research has shown moderate to large effects of PPOs on well-being in people with reduced wellbeing and psychological symptoms at baseline. The University of Twente developed an app (Training in Positivity; TiP) based on an effective intervention. The goal of this study is to investigate the effectiveness of TiP in the general population in people experiencing reduced mental wellbeing as a result of the corona crisis. People using the app will be compared to a waiting list control group.

Condition or Disease Intervention/Treatment Phase
  • Other: Training in positivity
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
306 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
A Randomized Controlled Trial on the Effectiveness of a Positive Psychology App for Adults in the General Population Dealing With Negatives Consequences of the Corona Crisis
Actual Study Start Date :
Apr 4, 2022
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Positive psychology app

Other: Training in positivity
The University of Twente developed an evidence-based positive psychology app that is aimed at increasing mental well-being and resilience (Training in positivity; TiP). TiP consists of a 3-week structured intervention, in which participants do two exercises every week for 6 days, aimed at increasing resilience and mental well-being. An exercise takes an average of 15 minutes per day.

Other: Waiting list

Other: Training in positivity
The University of Twente developed an evidence-based positive psychology app that is aimed at increasing mental well-being and resilience (Training in positivity; TiP). TiP consists of a 3-week structured intervention, in which participants do two exercises every week for 6 days, aimed at increasing resilience and mental well-being. An exercise takes an average of 15 minutes per day.

Outcome Measures

Primary Outcome Measures

  1. Mental well-being [Change from baseline mental well-being at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2).]

    Mental well-being measured with the 14-item Mental Health Continuum-Short Form. Scores are calculated as mean scores and can range from 0 to 5. Higher scores indicate more mental well-being.

Secondary Outcome Measures

  1. Ability to adapt [Change from baseline ability to adapt at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 10-item Generic sense of ability to adapt scale. Scores are calculated as sum scores and can range from 10 to 50. Higher scores indicate more ability to adapt.

  2. General self-efficacy [Change from baseline general self-efficacy at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 10-item General Self-Efficacy Scale. Scores are calculated as sum scores and can range from 10 to 40. Higher scores indicate more general self-efficacy.

  3. Savoring [Change from baseline savoring at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 24-item Savoring Beliefs inventory. Scores are calculated as mean scores and can range from 1 to 7. Higher scores indicate more savoring.

  4. Self-compassion [Change from baseline self-compassion at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 8-item self-reassurance subscale of the Forms of self-criticising/attacking & self-reassuring scale. Scores are calculated as mean scores and can range from 0 to 4. Higher scores indicate more self-compassion.

  5. Positive reframing [Change from baseline positive reframing at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with 2 items of the positive reframing subscale of the Coping Orientations and Problems Experienced inventory. Scores are calculated as mean scores and can range from 1 to 4. Higher scores indicate more positive reframing.

  6. Anxiety symptoms [Change from baseline anxiety symptoms at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 7-item Generalized Anxiety Disorder-7 questionnaire. Scores are calculated as sum scores and can range from 0 to 21. Higher scores indicate more anxiety symptoms.

  7. Depression symptoms [Change from baseline ability to adapt at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 9-item Patient Health Questionnaire-9. Scores are calculated as sum scores and can range from 0 to 27. Higher scores indicate more depression symptoms.

  8. Spiritual well-being [Change from baseline spiritual well-being at 3 weeks (T1) and change from baseline mental well-being at 3 months (T2)]

    Measured with the 7-item Spiritual Attitude and Involvement List-Short Form. Scores are calculated as mean scores and can range from 1 to 6. Higher scores indicate more spiritual well-being.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. The participant is at least 18 years old

  2. The participant has an e-mail address and is in possession of a smartphone or tablet with access to the internet.

  3. The participant is willing to do a positive psychology exercise 6 days a week for 3 weeks

  4. The participant has sufficient command of the Dutch language to be able to complete questionnaires and exercises.

  5. The participant gives consent to participate in the study using the online informed consent procedure.

Exclusion Criteria:
  1. The presence of severe anxiety symptoms: a score of 15 or higher on the Generalized Anxiety Disorder 7 items (GAD-7)

  2. The presence of severe depressive symptoms: a score of 20 or higher on the Patient Health Questionnaire (PHQ-9).

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Twente Enschede Overijssel Netherlands 7522NB

Sponsors and Collaborators

  • University of Twente

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jannis Kraiss, Assistant Professor, University of Twente
ClinicalTrials.gov Identifier:
NCT05292560
Other Study ID Numbers:
  • 220106
First Posted:
Mar 23, 2022
Last Update Posted:
Aug 19, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 19, 2022