ArticleJMIR research protocols2025
The Effects of a Smartphone App (Feelee) to Enhance Adolescents' Emotion Regulation Skills in a Forensic Outpatient Setting: Protocol for a Multiple Single-Case Experimental Design.
Article in JMIR research protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06509360 (How do You Feelee? Does an Ordinary Question a Day Supports Youth in a Forensic Outpatient Setting to Become More Emotional Balanced? A Multiple Case Experimental Design), which is not on this map. Cited by 1 paper.
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How do You Feelee? Does an Ordinary Question a Day Supports Youth in a Forensic Outpatient Setting to Become More Emotional Balanced? A Multiple Case Experimental Design
Who cites it
1 citing paper in PubMed.
- Trial
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5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDifficulties in emotion regulation are a significant contributing factor to delinquent behavior in adolescence. These adolescents struggle with recognizing, comprehending, and controlling emotions, which impedes the effectiveness of current forensic treatments. In addition, forensic care often faces challenges regarding treatment engagement due to a lack of motivation and difficulties building an alliance between clients and caregivers. The use of Feelee, an app that collects and displays active and passive data, is promising to support adolescents in obtaining more insight into their emotion regulation abilities. Furthermore, the integration of smartphone apps, like Feelee, offers new perspectives to increase adolescents' engagement and adherence to treatment.
objectiveThis study presents the research protocol for evaluating the initial effects of the Feelee app on emotion regulation among adolescents in the forensic outpatient setting. The Feelee app integrates with treatment as usual, and the multiple single-case experimental design methodology is discussed in detail.
methodsA multiple single-case experimental ABA design was applied to examine the initial effectiveness of Feelee. A total of 24 participants from 2 forensic outpatient care centers completed a 2-week baseline (phase A1), 4-week intervention (phase B), and a 2-week follow-up (phase A2). The primary outcome, emotional regulation, is measured daily using self-reports via the smartphone. Secondary outcomes, including emotional differentiation, insight and self-reflection, emotional awareness, and treatment-related factors such as motivation and therapeutic alliance, are assessed through questionnaires administered at preintervention, postintervention, and follow-up points. Quantitative analyses follow single-case experimental design methods, including visual analysis of individual trajectories, standardized mean difference permutation distance tests, and Cohen d at the group level. A 95% CI is calculated per participant to assess change reliability. Secondary outcomes are analyzed using the Reliable Change Index. Qualitative follow-up interviews are analyzed using thematic analysis at both the individual and group levels.
resultsData collection started in June 2023 and was completed in January 2025. By the time of final manuscript submission, 89 participants had been recruited and 24 had enrolled in the study. Study results will be published in peer-reviewed journals and presented at national and international conferences throughout 2025.
conclusionsThis study aims to evaluate the effectiveness of the Feelee app in enhancing emotion regulation skills. By using a multiple single-case experimental ABA design, we will get a first insight into the addition of Feelee to treatment as usual in the forensic outpatient setting. Study strengths include the low-threshold addition, ecological validity, and the use of both quantitative and qualitative research methods. Further implications for clinical practice are discussed.
trial registrationCentral Committee on Research Involving Human Subjects NL-OMON54390; https://onderzoekmetmensen.nl/en/trial/54390 and ClinicalTrials.gov NCT06509360; https://clinicaltrials.gov/study/NCT06509360. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/64756.
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