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Not yet recruiting NCT04210648

Effectiveness and Security Testing of a Mobile App for Self-Managing Emotion Dysregulation

No phase Interventional Emotional Dysregulation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mobile app.
Who it may be relevant to
Registry conditions: Emotional Dysregulation. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Effectiveness and Security Testing of a Mobile App for Self-Managing Emotion Dysregulation in a Non-Clinical Population With Borderline Traits: A Randomized Controlled Trial

Overview

To assess the effectiveness and security of a mobile App (beta version) for people with borderline traits recruited from a non-clinical population of college students in Barcelona (Spain). The main primary outcome will be the severity of the emotional dysregulation. Forty participants will use the mobile app over 6 months. This group while be compared at post-treatment and at 3-month follow-up with other 40 participants (control group) with any intervention.

Interventions

  • Device Mobile app
    Mobile app for self-managing emotional dysregulation

Primary outcome measures

  • Emotion dysregulation severity [Time frame: 9-month]
  • smartphone addiction [Time frame: 9-month]

Eligibility criteria

Inclusion criteria

  • Borderline traits
  • Aged between 18 to 65 years
  • College students

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT04210648 · 32-16

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗