Effects of a Relaxation and Guided Imagery Intervention in School Context

NCT06101225 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2023-11-07

No results posted yet for this study

Summary

Specific aims - To test the effects of a relaxation and guided imagery intervention with socioemotional learning content on a range of socioemotional, physiological, cognitive and academic outcomes of school-aged children, measured through self-reports, neuropsychological and physiological measures, as well as teachers and parent's reports.

Conditions

  • Mental Health Wellness 1
  • Positive and Negative Affect
  • Social Skills
  • Happiness
  • Self Esteem
  • Self-Regulation, Emotion
  • Anxiety
  • Cognitive Change
  • Heart Rate Variability
  • Stress, Psychological
  • Physical Activity

Interventions

OTHER

MindRegulation Intervention

The intervention is developed in class for 15 minutes before learning activities, three times per week, for five months - 57 sessions. Six different scripts with socioemotional learning content (based on CASEL framework) for each of the three themes will be applied.

OTHER

Relaxation

The relaxation condition will be developed in the same way as in RegularMente intervention, but without the guided imagery with SEL component. Relaxation exercises applied in class 15 minutes before learning activities, three times per week, for five months - in a total of 57 sessions.

OTHER

Waiting List Control Group

No Intervention.

Sponsors & Collaborators

  • Faculdade de Psicologia, Universidade de Lisboa

    collaborator UNKNOWN
  • ISCTE-IUL

    collaborator UNKNOWN
  • ISAMB - Faculdade de Medicina da Universidade de Lisboa

    collaborator UNKNOWN
  • Technical University of Lisbon

    collaborator OTHER
  • Universidade Católica Portuguesa

    collaborator OTHER
  • Universidade Lusófona de Humanidades e Tecnologias

    collaborator OTHER
  • Universidade Nova de Lisboa

    collaborator OTHER
  • Universidade Autónoma de Lisboa

    lead OTHER

Principal Investigators

  • Iolanda C. Galinha, Phd · Universidade Autónoma de Lisboa

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
7 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-10-09
Primary Completion
2025-07-30
Completion
2026-06-30

Countries

  • Portugal

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06101225 on ClinicalTrials.gov