The Caring Universities Project: EsteemUp RCT

Sponsor
VU University of Amsterdam (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05582954
Collaborator
Erasmus University Rotterdam (Other), University of Amsterdam (Other), Leiden University (Other), Maastricht University (Other), Utrecht University (Other), InHolland University of Applied Sciences (Other)
356
1
2
11.9
29.9

Study Details

Study Description

Brief Summary

Within the Caring Universities project (study protocol VCWE- 2020-135 accepted by the VCWE), the investigators have developed a guided e-health programme (EsteemUp) designed to increase university students' self-esteem. With the current study, the investigators aim to examine the feasibility and acceptability of EsteemUp - with and without gamification elements - to improve students' self-esteem.

Secondary goals are to gain insight into pre-test to post-test differences regarding self-esteem, symptoms of depression, anxiety and quality of life.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: EsteemUp
  • Behavioral: EsteemUp-G
N/A

Detailed Description

The present study is a two-armed randomized controlled trial. This trial will be conducted in a university setting. Participants will be randomized to receive a version of the intervention either with gamification elements (EsteemUp-G) or without gamification elements (EsteemUp).

EsteemUp was developed based on existing literature on self-esteem and adapted in collaboration with university students to meet the specific needs of the university students. EsteemUp is based on cognitive-behavioural therapy (CBT) and consists of four modules that are delivered via computer, laptop, tablet, or mobile phone. Every module consists of evidence-based information, exercises, and homework assignments. The content is delivered in text format with pictures and infographics. The intervention is available in both English and Dutch.

Participants assigned to EsteemUp-G will receive the exact same intervention explained above with an addition of gamification elements. These elements include Badges, unlockable content,

  1. certification of completion at the end of the program, goal setting, gamification terminology and a progress bar.

Every week trained e-coaches (trained clinical psychology master students) will provide asynchronous written personalized feedback to each participant on the progress of the program and the exercises via the program platform. Measurements include post-test assessment of adherence, treatment satisfaction, and satisfaction with e-coach. Secondary outcomes include pre and post-assessment of self-esteem, common measures of psychopathology symptoms, and quality of life.

Data will be analysed based on the intent-to-treat principle.

All students currently enrolled at the participating universities (Vrije Universiteit Amsterdam, Erasmus University, InHolland University of Applied sciences, Universities of Amsterdam, Leiden, Utrecht and Maastricht) are potentially eligible for the trial.

Students can participate in EsteemUp free of charge, which will likely increase their self-esteem and confidence. They will not receive any additional incentives for participation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
356 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The present study is a two-armed randomized controlled trial. This trial will be conducted in a university setting. A guided web-based intervention to improve self-esteem (EsteemUp) will be compared to a version of the same intervention with gamification elements (EsteemUp-G)The present study is a two-armed randomized controlled trial. This trial will be conducted in a university setting. A guided web-based intervention to improve self-esteem (EsteemUp) will be compared to a version of the same intervention with gamification elements (EsteemUp-G)
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
An independent researcher who is not involved in the study will generate the random sequence using a computer random sequence generator. Randomisation will take place at an individual level, stratified by gender and the university where students study. Participants will be randomised into two groups (EsteemUp vs EsteemUp-G) with an allocation ratio of 1:1. We will conduct block randomisation with randomly varied block sizes (6 to 12 allocations per block) to prevent foreknowledge of intervention assignment. Allocation will be concealed from the study's researchers. It is not possible to mask personnel and participants to the treatment allocation because of the nature of the intervention.
Primary Purpose:
Treatment
Official Title:
Feasibility and Acceptability of a Guided E-health Programme (EsteemUp), With and Without Gamification Elements, to Increase Self-esteem in University Students.
Actual Study Start Date :
Nov 3, 2022
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: EsteemUp

Participants assigned to this arm will receive a 4 week-guided e-health application - EsteemUp - to improve their self-esteem

Behavioral: EsteemUp
EsteemUp is a guided e-health application based on cognitive-behavioural therapy (CBT). It consists of four modules that take approximately 30 to 45 minutes to complete. Each module includes evidence-based psycho-education, reflection questions, interactive exercises, and homework assignments. The content is delivered both textually and visually, including the use of pictures, infographics and videos. Every week trained e-coaches (trained clinical psychology master students) will provide asynchronous written personalized feedback to each participant on the progress of the program and the exercises via the program platform.

Active Comparator: EsteemUp -G

This group will receive the same intervention (EsteemUp) with the addition of gamification elements.

Behavioral: EsteemUp
EsteemUp is a guided e-health application based on cognitive-behavioural therapy (CBT). It consists of four modules that take approximately 30 to 45 minutes to complete. Each module includes evidence-based psycho-education, reflection questions, interactive exercises, and homework assignments. The content is delivered both textually and visually, including the use of pictures, infographics and videos. Every week trained e-coaches (trained clinical psychology master students) will provide asynchronous written personalized feedback to each participant on the progress of the program and the exercises via the program platform.

Behavioral: EsteemUp-G
The gamification elements added to this arm include (1) Badges - digital rewards upon completing important milestones within the programme EsteemUp. (2) Unlockable content - downloadable worksheets of the exercises that they have done in the module, (3) A certification of completion at the end of the program, (4) Goal setting (5) Gamification terminology - All homework assignments will be framed as a 'challenge' that needs to be completed, (6) a progress bar that will indicate how far along the participant is in the program

Outcome Measures

Primary Outcome Measures

  1. Satisfaction with the intervention [T1 (post test: 4-weeks)]

    The Client Satisfaction Questionnaire (CSQ-8) is used to measure participants' satisfaction with the overall intervention. The CSQ-8 is commonly used to measure satisfaction with online interventions. It consists of eight items on a four-point Likert scale with a total score ranging from 8 to 32, where a higher score indicates greater satisfaction.

  2. Treatment Adherence [T1 (post test: 4-weeks)]

    Adherence refers to "the degree to which the user followed the program as it was designed" (Donkin et al., 2011). The present study measures adherence by dividing the number of modules completed by a participant at time of post-test by the total number of modules in the programme, and multiplying this by 100. The resulting percentage will indicate completion rate.

  3. Satisfaction with E-coach [T1 (post test: 4-weeks)]

    The Working Alliance Inventory for guided internet interventions (WAI-I) is used to evaluate participant's satisfaction with the e-coach. The WAI-I consists of 12 items on a 5-point Likert scale with a total score ranging from 12 to 60, where higher scores indicate higher satisfaction

Secondary Outcome Measures

  1. Change in self-esteem [T0 (Baseline) to T1 (Post-test: 4-weeks)]

    The Rosenberg Self-Esteem Scale (RSS) is used to measure explicit self-esteem. This tool consists of 10 items measured on a four-point Likert scale ranging from 1(strongly disagree) to 4(strongly agree). The total scores range from 10 to 40 with higher scores indicating better self-esteem.

  2. Change in depressive symptoms [T0 (Baseline) to T1 (Post-test: 4-weeks)]

    The Patient Health Questionnaire (PHQ-9) is used as the measure of depression. This questionnaire consists of 9 items scored on a four-point Likert scale ranging from 0 (not at all) to 3 (nearly every day). The total scores can range from 0 to 27, with higher scores indication more severe depressive symptoms

  3. Change in Anxiety symptoms [T0 (Baseline) to T1 (Post-test: 4-weeks)]

    The Generalized Anxiety Disorder scale (GAD-7) is used to measure symptoms of generalized anxiety. The questionnaire consists of 7 items measured on a four-point Likert ranging from 0 (not at all) to 3 (nearly every day). The total scores range from 0 to 21 with higher scores indicating more severe GAD symptoms

Other Outcome Measures

  1. Socio demographic characteristics of participants [T0 (Baseline)]

    age gender ethnicity student status study level relationship status whether the student is currently undergoing any treatment (pharmacotherapy/psychotherapy/both/none)

  2. Satisfaction with individual modules [Module 1, Module 2, Module 3, Module 4]

    After completing each module, the participants respond to the question "how useful was this module" on a scale of 1 - 100, with higher scores indicating better satisfaction with the module.

  3. Satisfaction with badges [T1 (Post-test: 4-weeks)]

    Satisfaction with the badges is measured after completing EsteemUp-G. Participants respond to 3 statements measured on a five-point Likert scale ranging from 0 (strongly disagree) to 4 (strongly agree). These statements are: "The badges were a good addition to the program", "I enjoyed collecting the badges", and "the badges increased my motivation to keep working on the program". The total satisfaction score ranges from 0 to 12, with higher scores indicating greater satisfaction with the badges.

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

To be eligible to participate in this trial, a subject must meet all the following criteria:

  • Being fluent in Dutch and/or English

  • Being enrolled as a student of the seven participating universities

  • Being 16 years of age or older

  • Having access to a PC or mobile device with internet access

  • Provide informed consent before participation

Exclusion Criteria:
  • None. All interested students are eligible to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vrije Universiteit Amsterdam Amsterdam Netherlands 1181 HV

Sponsors and Collaborators

  • VU University of Amsterdam
  • Erasmus University Rotterdam
  • University of Amsterdam
  • Leiden University
  • Maastricht University
  • Utrecht University
  • InHolland University of Applied Sciences

Investigators

  • Study Director: Pim Cuijpers, dr. Prof, VU University of Amsterdam

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Arpana Amarnath, Associate Researcher, VU University of Amsterdam
ClinicalTrials.gov Identifier:
NCT05582954
Other Study ID Numbers:
  • VCWE-2022-135
First Posted:
Oct 17, 2022
Last Update Posted:
Nov 30, 2022
Last Verified:
Nov 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 30, 2022