- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06419933
Emotional Problems in Preschool Children: Evaluation of the SuperKids Program (PRE-KIDS)
April 3, 2025 updated by: Mireia Orgilés Amorós, Universidad Miguel Hernandez de Elche
Prevention of Emotional Problems in Preschool Children Aged to 4 to 6 Years Old: Evaluation of the SuperKids Program (PRE-KIDS)
Emotional problems are among the most frequent psychological problems in the school stage, having an early onset.
When they are not detected and they do not receive adequate intervention, they persist and become chronic, being considered precursors of other problems in adolescence and adulthood.
The early onset of emotional problems, and their precursor role for other disorders, justify the need for preventive interventions as soon as possible.
Since there is evidence that anxiety and depression share common underlying mechanisms, preventive programs should address shared risk factors.
For this reason, the objective of this study is to test the effectiveness of an 8-session cognitive-behavioral protocol developed for Spanish children aged 4 to 6 in the educational context in a controlled trial.
The objective of the program is that children improve their skills to manage their own emotions and to improve their ability to interact with other.
The program will be applied ina group format and will be enriched with multimedia material that the implementer will project at various moments of the sessions.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
A 2 x 3 factorial design will be used, with the intervention variable as an intergroup factor (intervention or waiting list), and with the evaluation phase as an intragroup factor (pretest, posttest, 12 months follow-up).
Parents and children will complete the same measures at baseline, post-treatment, and follow-up.
The investigators will compare the results of pre- and post-assessments of children participating in the program on emotional and social variables.
Study Type
Interventional
Enrollment (Estimated)
500
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Marina Serrano Ortiz
- Phone Number: +34965222071
- Email: marina.serranoo@umh.es
Study Contact Backup
- Name: Mireia Orgilés Amorós
- Phone Number: +34 96 665 8348
- Email: morgiles@umh.es
Study Locations
-
-
Alicante
-
Elche, Alicante, Spain, 03202
- Recruiting
- Department of Health Psychology. Miguel Hernandez University of Elche Elche, Alicante, Spain, 03202
-
Contact:
- Marina Serrano Ortiz
- Phone Number: +34965222071
- Email: marina.serranoo@umh.es
-
Contact:
- Mireia Orgilés Amorós
- Phone Number: +34 96 665 8348
- Email: maorgiles@umh.es
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Children aged 4 to 6 years.
Exclusion Criteria:
- Intellectual disability, behavioral symptoms or autistic spectrum symptoms whose severity prevented the continuation of treatment.
- Current psychological or pharmacological treatment for anxiety and/or depression.
- Not accepting or revoking informed consent to participate in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group wait-list
Group without any intervention.
Participants in the wait-list group will receive no psychological intervention during the eight-week duration of the SuperKids program.
Families will be informed that children in this group will receive the intervention once the follow-up is completed.
|
|
|
Experimental: Experimental group
SuperKids Structured and manualized intervention with a manual for the therapist and a workbook for the children.
The intervention will be administered by SuperKids-trained clinical psychologists.
Sessions will take place once a week for eight weeks, with each session lasting approximately forty-five minutes.
The program includes emotional education and social skills training.
These contents are learned through playful exercises, activities, readings and role-playing.
The intervention modality will be face-to-face.
|
The SuperKids program will be administered following the manual of the intervention by a trained therapist, as described in the section of intervention/ treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Kiddy-KINDL-R
Time Frame: Before starting the study
|
Baseline level of physical and emotional well-being reported by parents as measured by the Kiddy-KINDL-R questionnaire.
The Kiddy-KINDL-R measures assesses physical and emotional well-being of children aged 4 to 7 years across six dimensions: physical well-being, psychological well-being, self-esteem, family, social relationships, and school.
Parents rate each item on a 5-point Likert scale: never (1), almost never (2), sometimes (3), almost always (4), and always (5).
The total score is calculated by adding the scores for each dimension (range for each dimension: 4 to 20 points).
Higher scores on each subscale and on the total scale indicate higher symptoms in children.
|
Before starting the study
|
|
The Kiddy-KINDL-R
Time Frame: Immediately after the intervention.
|
Level of physical and emotional well-being reported by parents immediately after the intervention measured by the Kiddy-KINDL-R questionnaire.
The Kiddy-KINDL-R measures assesses physical and emotional well-being of children aged 4 to 7 years across six dimensions: physical well-being, psychological well-being, self-esteem, family, social relationships, and school.
Parents rate each item on a 5-point Likert scale: never (1), almost never (2), sometimes (3), almost always (4), and always (5).
The total score is calculated by adding the scores for each dimension (range for each dimension: 4 to 20 points).
Higher scores on each subscale and on the total scale indicate higher symptoms in children.
|
Immediately after the intervention.
|
|
The Kiddy-KINDL-R
Time Frame: 12 months after the intervention.
|
Level of physical and emotional well-being reported by parents at 12 months Measured by the Kiddy-KINDL-R questionnaire.
The Kiddy-KINDL-R measures assesses physical and emotional well-being of children aged 4 to 7 years across six dimensions: physical well-being, psychological well-being, self-esteem, family, social relationships, and school.
Parents rate each item on a 5-point Likert scale: never (1), almost never (2), sometimes (3), almost always (4), and always (5).
The total score is calculated by adding the scores for each dimension (range for each dimension: 4 to 20 points).
Higher scores on each subscale and on the total scale indicate higher symptoms in children.
|
12 months after the intervention.
|
|
Preschool Spence Anxiety Scale (PAS)
Time Frame: Before starting the study
|
Baseline child-reported anxiety symptoms as measured by the Preschool Spence Anxiety Scale (PAS).
The PAS measures symptom severity of DSMIV anxiety disorders in children (subscales: total, panic and agoraphobia, generalized anxiety disorder, obsessive-compulsive disorder, social phobia, separation anxiety, and specific fears).
The frequency of symptoms is recorded on a 3-point Likert scale from 0 (never) to 3 (always).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater symptom severity.
Higher scores indicate greater symptom severity.
|
Before starting the study
|
|
Preschool Spence Anxiety Scale (PAS)
Time Frame: Immediately after the intervention.
|
Anxiety symptoms reported by children immediately after the intervention measured using the Spence Preschool Anxiety Scale, (PAS).
The PAS measures symptom severity of DSMIV anxiety disorders in children (subscales: total, panic and agoraphobia, generalized anxiety disorder, obsessive-compulsive disorder, social phobia, separation anxiety, and specific fears).
The frequency of symptoms is recorded on a 3-point Likert scale from 0 (never) to 3 (always).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater symptom severity.
Higher scores indicate greater symptom severity.
|
Immediately after the intervention.
|
|
Preschool Spence Anxiety Scale (PAS)
Time Frame: 12 months after the intervention.
|
Child-reported anxiety symptoms at 12 months Measured using the Spence Preschool Anxiety Scale (PAS).
The PAS measures symptom severity of DSMIV anxiety disorders in children (subscales: total, panic and agoraphobia, generalized anxiety disorder, obsessive-compulsive disorder, social phobia, separation anxiety, and specific fears).
The frequency of symptoms is recorded on a 3-point Likert scale from 0 (never) to 3 (always).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater symptom severity.
Higher scores indicate greater severity of symptoms.
|
12 months after the intervention.
|
|
the Strengths and Difficulties Questionnaire
Time Frame: Before starting the study
|
Baseline Parent-reported depressive symptoms as measured by the Strengths and Difficulties Questionnaire, parent version (SDQ; Goodman, 1997).
The SDQ measure examines emotional difficulties (5 items), conduct problems (5 items), hyperactivity (5 items), peer problems (5 items), and prosocial behavior (5 items) in children aged 3 to 16 years.
Symptom frequency is recorded on a 3-point Likert scale from 0 (Not true) to 3 (Absolutely true).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater severity of symptoms.
Higher scores indicate greater symptom severity.
|
Before starting the study
|
|
the Strengths and Difficulties Questionnaire
Time Frame: Immediately after the intervention.
|
Depressive symptoms reported by parents inmediately after intervention measured by the Strengths and Difficulties Questionnaire, parent version (SDQ; Goodman, 1997).
The SDQ measure examines emotional difficulties (5 items), conduct problems (5 items), hyperactivity (5 items), peer problems (5 items), and prosocial behavior (5 items) in children aged 3 to 16 years.
Symptom frequency is recorded on a 3-point Likert scale from 0 (Not true) to 3 (Absolutely true).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater severity of symptoms.
Higher scores indicate greater symptom severity.
|
Immediately after the intervention.
|
|
the Strengths and Difficulties Questionnaire
Time Frame: 12 months after the intervention.
|
Depressive symptoms reported by parents at 12 months as measured by the Strengths and Difficulties Questionnaire, parent version (SDQ; Goodman, 1997).
The SDQ measure examines emotional difficulties (5 items), conduct problems (5 items), hyperactivity (5 items), peer problems (5 items), and prosocial behavior (5 items) in children aged 3 to 16 years.
Symptom frequency is recorded on a 3-point Likert scale from 0 (Not true) to 3 (Absolutely true).
A minimum possible score of 0 and a maximum possible score of 114 is obtained.
Higher scores indicate greater severity of symptoms.
Higher scores indicate greater symptom severity.
|
12 months after the intervention.
|
|
Behavioral Inhibition Questionnaire (BIQ
Time Frame: Before starting the study
|
Baseline of children's behavioral inhibition measured using the Behavioral Inhibition Questionnaire (BIQ).
The BIQ assesses the frequency of children's behavioral inhibition in six contexts across three domains: social novelty (unknown adults, peers, and performance in front of others), situational novelty (unfamiliar situations, preschool/separation), and novel physical activities with a possible risk of injury.
This questionnaire has 30 items that are scored on a seven-point scale ranging from 1 (almost never) to 7 (almost always).
Item scores are summed to create six scale scores: Unknown Peers, Unknown Adults, Performance Situations, Separation/Preschool, Unknown Situations, and Physically Challenging Situations.
|
Before starting the study
|
|
Behavioral Inhibition Questionnaire (BIQ
Time Frame: Immediately after the intervention.
|
Children's behavioral inhibition was immediately measured after the intervention using the Behavioral Inhibition Questionnaire (BIQ).
The BIQ assesses the frequency of children's behavioral inhibition in six contexts across three domains: social novelty (unknown adults, peers, and performance in front of others), situational novelty (unfamiliar situations, preschool/separation), and novel physical activities with a possible risk of injury.
This questionnaire has 30 items that are scored on a seven-point scale ranging from 1 (almost never) to 7 (almost always).
Item scores are summed to create six scale scores: Unknown Peers, Unknown Adults, Performance Situations, Separation/Preschool, Unknown Situations, and Physically Challenging Situations.
|
Immediately after the intervention.
|
|
Behavioral Inhibition Questionnaire (BIQ
Time Frame: 12 months after the intervention.
|
Children's behavioral inhibition was measured at 12 months using the Behavioral Inhibition Questionnaire (BIQ).
The BIQ assesses the frequency of children's behavioral inhibition in six contexts across three domains: social novelty (unknown adults, peers, and performance in front of others), situational novelty (unfamiliar situations, preschool/separation), and novel physical activities with a possible risk of injury.
This questionnaire has 30 items that are scored on a seven-point scale ranging from 1 (almost never) to 7 (almost always).
Item scores are summed to create six scale scores: Unknown Peers, Unknown Adults, Performance Situations, Separation/Preschool, Unknown Situations, and Physically Challenging Situations.
|
12 months after the intervention.
|
|
Parental Overprotection Scale
Time Frame: Baseline
|
Parental overprotective behavior is assessed with the Parental Overprotection Scale (OP, Edwards et al., 2008).
POM evaluates, through 19 items, the overprotective behavior of parents towards their children, related in previous studies to anxiety in preschool children.
Symptom frequency is recorded on a 3-point Likert scale, from 0 (not at all) to 4 (very much).
|
Baseline
|
|
Depression Anxiety Stress Scales - short version (DASS-21)
Time Frame: Baseline
|
Baseline parental depression, anxiety and stress symptoms Measured by the Depression Anxiety Stress Scales - short version (DASS-21).
It contains a set of three self-report scales designed to measure the emotional states of depression, anxiety and stress.
Each of the three DASS-21 scales contains 7 items, divided into subscales with similar content.
The depression scale assesses dysphoria, hopelessness, devaluation of life, self-deprecation, lack of interest / involvement, anhedonia and inertia.
The anxiety scale assesses autonomic arousal, skeletal muscle effects, situational anxiety, and subjective experience of anxious affect.
The stress scale is sensitive to levels of chronic nonspecific arousal.
It assesses difficulty relaxing, nervous arousal, and being easily upset / agitated, irritable / over-reactive and impatient.
Scores for depression, anxiety and stress are calculated by summing the scores for the relevant items.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Mireia Orgilés Amorós, Universidad Miguel Hernandez de Elche
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Bishop G, Spence SH, McDonald C. Can parents and teachers provide a reliable and valid report of behavioral inhibition? Child Dev. 2003 Nov-Dec;74(6):1899-917. doi: 10.1046/j.1467-8624.2003.00645.x.
- Orgiles M, Melero S, Penosa P, Espada JP, Morales A. [Parent-reported Health-Related Quality of Life in Spanish pre-schoolers: Psychometric properties of the Kiddy-KINDL-R]. An Pediatr (Engl Ed). 2019 May;90(5):263-271. doi: 10.1016/j.anpedi.2018.04.019. Epub 2018 Jul 6. Spanish.
- Orgiles M, Penosa P, Fernandez-Martinez I, Marzo JC, Espada JP. Spanish validation of the Spence Preschool Anxiety Scale. Child Care Health Dev. 2018 Sep;44(5):753-758. doi: 10.1111/cch.12593. Epub 2018 Jul 22.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2023
Primary Completion (Estimated)
July 30, 2025
Study Completion (Estimated)
August 1, 2025
Study Registration Dates
First Submitted
May 8, 2024
First Submitted That Met QC Criteria
May 14, 2024
First Posted (Actual)
May 17, 2024
Study Record Updates
Last Update Posted (Actual)
April 8, 2025
Last Update Submitted That Met QC Criteria
April 3, 2025
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- PID2021-126473NB-I00
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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