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Emotion Regulation Group Study

Emotion Regulation Group Intervention for Late Adolescents: a Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05734677
Acronym
EmoReg
Enrollment
56
Registered
2023-02-21
Start date
2022-01-01
Completion date
2023-12-31
Last updated
2023-02-21

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

Conditions

Borderline Personality Disorder, Emotional Dysfunction

Brief summary

A clinical trial to evaluate the effects of an eight-week emotion regulation group intervention designed for adolescents (16-20 years old) on the levels of emotion dysregulation both self-reported by the adolescent and reported by his/her parent/caregiver (pre-post comparison). The long-term effect will also be measured at a third-time point, three months after the end of the intervention. The intervention will consist of 90-minute sessions once a week for 8 weeks, in groups of eight participants. The intervention proposed for this study is an adaptation from different interventions already in use for adolescents in clinical practice, such as Dialectical Behavior Therapy (DBT), Mentalization-Based Treatment (MBT) and Mindfulness-Based Intervention (MBI).

Interventions

BEHAVIORALEmotion regulation group

90 minute sessions once a week for 8 weeks, in groups of eight participants. DBT, MBT and MBI inspired, psychoeducative intervention.

Sponsors

Fondation Privée des HUG
CollaboratorUNKNOWN
Camille Nemitz Piguet
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged between 16 to 20 years old. * \> 4 criteria of borderline symptoms (out of the 9 listed in the DSM-5) including emotional liability * French speaking * Availability during the whole study * Willingness in participating to the intervention and the research * Informed consent read and signed

Exclusion criteria

* Current hospitalization * Psychotic disorder * Severe and persistent substance addiction * Antisocial personality disorder * Inability to participate in group sessions * Current pregnancy * Non-French speaking * Previous enrolment into the current study

Design outcomes

Primary

MeasureTime frameDescription
Changes from Baseline in Difficulties in emotion regulation scale (DERS)V2 (within two weeks after the end of the intervention)36 items self-report scale: Higher scores suggest greater problems with emotion regulation.
Changes from Baseline in Emotion Dysregulation Inventory (EDI)V2 (within two weeks after the end of the intervention)Informant-report measure of emotion dysregulation

Secondary

MeasureTime frameDescription
Changes from Baseline in self-report Family Attitude Scale (FAS)V2 (within two weeks after the end of the intervention)30-item, Likert-scaled assessment for measuring the emotional climate of families (higher score = more critical family environment)
Changes from Baseline in parent-report Family Attitude Scale (FAS)V2 (within two weeks after the end of the intervention)30-item, Likert-scaled assessment for measuring the emotional climate of families (higher score = more critical family environment)
Changes from Baseline in Borderline Symptom List (BSL-23)V2 (within two weeks after the end of the intervention)Self-rating tool for Borderline Personality Disorder (BPD) symptoms: higher scores = more likely to have BPD and associated challenges
Changes from Baseline in self-report Strength & Difficulties Questionnaire (SDQ)V2 (within two weeks after the end of the intervention)brief emotional and behavioural screening questionnaire assessing 25 attributes, some positive and others negative.
Changes from Baseline in Beck Depression Inventory (BDI-II)V2 (within two weeks after the end of the intervention)Self-report inventory scored from 0 to 63 (higher score = more severe depressive symptoms)
Changes from Baseline in Cognitive Emotion Regulation Questionnaire (CERQ)V2 (within two weeks after the end of the intervention)Self-report measure designed to assess individual differences in cognitive regulation of emotions in response to stressful events. subscale scores can range from 4 to 20 with higher subscale scores indicating greater frequency of use of the specific cognitive strategy.
Changes from Baseline in Kentucky inventory of mindfulness skills (KIMS)V2 (within two weeks after the end of the intervention)self-report measuring Mindfulness on four scales: Observing, Describing, Act With Awareness, and Accept Without Judgment. Higher scores = higher mindfulness
Changes from Baseline in Perceived Parental Autonomy Support Scale (P-PASS)V2 (within two weeks after the end of the intervention)Measures parental autonomy-support and control of late adolescents and emerging adults. 24 items, assessed on a 7 point Likert scale.
Changes from Baseline in parent-report Strength & Difficulties Questionnaire (SDQ)V2 (within two weeks after the end of the intervention)brief emotional and behavioural screening questionnaire assessing 25 attributes, some positive and others negative.
Changes from Baseline in State-Trait Anxiety Inventory (STAI)V2 (within two weeks after the end of the intervention)40 self-report items on a 4-point Likert scale: higher scores = greater anxiety

Countries

Switzerland

Contacts

Primary ContactCamille Piguet
camille.piguet@unige.ch+41 79 668 75 07

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026