Body-oriented Interventions on Preschoolers' Social-emotional Competence

February 15, 2023 updated by: Andreia Dias Rodrigues, University of Évora

Effects of Three Body-oriented Intervention Programs on Preschoolers' Social-emotional Competence

Experimental study with 4 groups (3 experimental and 1 control). Examine the effects of 3 body-oriented intervention programs on preschoolers' social-emotional competence.

Intervention programs focused on relaxation, loose parts play and combined loose parts play and relaxation, for 12 weeks with 2 30-min sessions per week.

Study Overview

Detailed Description

To examine the chronic effects of the intervention programs, instruments were collected at baseline (pretest) and at the end of the 12-week period (post-test). To measure the acute effects, salivary cortisol was measured at the beginning and end of the 1st and the 24th sessions.

Study Type

Interventional

Enrollment (Actual)

62

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 Locations

      • Évora, Portugal, 7000-847
        • Andreia Dias Rodrigues

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

3 years to 6 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • participants' age between 3 and 6 years
  • do not have participated in a similar intervention program within the last 6 months
  • do not have a physical condition that can affect the participation in the program.

Exclusion Criteria:

  • participants' age less than 3 and under 6 years
  • have participated in a similar intervention program within the last 6 months
  • have a physical condition that can affect the participation in the program.

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: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Relaxation group
Relaxation program sessions had 3 phases: initial dialogue (2 min); a main section (25 min); final ritual (3 min). During the main section, participants listened and observed the therapist, who described and demonstrated all the exercises of the session, which were focused on Jacques Choque Method (Choque, 1994).
Sessions focused on relaxations activities (Jacques Choque Method).
Experimental: Loose parts play group
Loose Parts Play program sessions had 3 phases: initial dialogue (2 min); main section (25 min); final ritual (3 min). During the main section, participants were allowed to play freely with any materials (loose parts) available in the playground.
Loose parts play-based sessions, with open-ended materials.
Experimental: Combined group
In the combined program, the sessions had 4 phases: initial dialogue (3 min); loose parts play moment (20 min); relaxation exercises moment (5 min); final ritual (2 min).
Sessions focused on loose parts play and relaxation activities.
No Intervention: Control group
No intervention. Maintained their usual routines.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Emotion discrimination
Time Frame: 1 and 12 weeks
Emotion discrimination was measured through the Emotion-discrimination Task. This measurement consists in two performance tasks of increasing difficulty. In the task 1 (neutral condition) children were tested on their ability to discriminate between cars and flowers, and faces with hats versus faces with glasses. This neutral condition is not scored, since is used to check if children understood how to sort different cards. In task 2, children had a sheet in front of them with a sample drawing of one category in the top left corner (e.g. an angry face) and a drawing of the other category in the top right corner (e.g. a sad face). Then, children have six cards (with the same emotion) and one by one they have to place each card in the correct category after a demonstration. The cards that were placed correctly were counted with 1 point, with a maximum of 3 points.
1 and 12 weeks
Change in Emotion identification
Time Frame: 1 and 12 weeks
Emotion identification was measured through the Emotion-identification Task. The task consists of eight drawings of facial emotion expressions, two for each emotion (happiness, sadness, fear, and anger). Then the researcher show two sheets with four drawings of facial emotion expressions on each sheet and ask to the children: "Who looks happy?", and children have to point to the drawing with the correct facial expression. Next, the researcher ask if "Is there anybody else who looks happy?". This procedure is repeated for anger, sadness, and fear. The number of emotions correctly identified was recorded, with a maximum score of 2 per emotion.
1 and 12 weeks
Change in Emotion recognition
Time Frame: 1 and 12 weeks
Emotion recognition was measured thought the subscale Others' Emotion Recognition (6 items) of the Portuguese version of the Emotion Expression Questionnaire. This Subscale indicates the extent to which the child can recognise the parents' and others' emotions. Parents can rate to what degree each item is true on a 5-point scale (0=(almost) never, 1=rarely, 2=sometimes, 3=often, 4=(almost) always).
1 and 12 weeks
Change in Positive and negative emotion expression
Time Frame: 1 and 12 weeks
Positive emotion expression, and negative emotion expression was measured through the Negative Emotion Expression subscale (8 items) and Positive Emotion Expression subscale (6 items) from the EEQ. Parents scored on a 5-point scale (0=(almost) never, 1=rarely, 2=sometimes, 3=often, 4=(almost) always), the frequency, intensity, and duration of child's expressions of negative emotions (e.g., anger, sadness), and positive emotions (e.g., happiness, joy). The extent to which the child can calm down from the emotional episode was also measured (1=easy; 3= difficult).
1 and 12 weeks
Change in Self-regulation
Time Frame: 1 and 12 weeks
Self-regulation was measured through the Portuguese version of Head-Toes-Knees-Shoulders Task (HTKS). Using no materials, the HTKS has three sections with up to four paired behavioral rules: "touch your head" and "touch your toes"; "touch your shoulders" and "touch your knees". Child first respond naturally, but then had to perform the opposite of a dominant response (e.g., touch your head when the interviewer says "touch your toes"). This task includes three phases (each with 10 trials), and for each trial, the child received a score of 0 (incorrect), 1 (self-correct), or 2 (correct).
1 and 12 weeks
Change in Stress regulation
Time Frame: 2 days
Stress regulation was measured through cortisol levels (mcg/dL) was quantified in saliva samples collected at the same time and in the same place where the interventions occurred, before and after the 1st and 24th sessions. Samples were collected directly from each child's mouth, without stimulation, by passive droll during 5 minutes to a polyethylene tube.
2 days
Change in Social competence
Time Frame: 1 and 12 weeks
Social competence was obtained through the prosocial behaviors scale (5 items), and positive items from the peer problems scale (2 items) of the Portuguese version of Strengths and Difficulties Questionnaire (SDQ). Rated on a 3-point scale (0 = not true, 1 = somewhat true, and 2 = certainly true) the degree to which each item represented child's behavior in the last 3 months.
1 and 12 weeks
Change in Externalizing problems
Time Frame: 1 and 12 weeks
Externalizing problems was obtained also through the behavior problems scale (5 items), and hyperactivity scale (5 items) of the Strengths and Difficulties Questionnaire (SDQ). Rated on a 3-point scale (0 = not true, 1 = somewhat true, and 2 = certainly true) the degree to which each item represented child's behavior in the last 3 months.
1 and 12 weeks
Change in Conflicts resolution
Time Frame: 1 and 12 weeks
Conflicts resolution was measured through the conflict resolution strategies subscale (6 items) of the Portuguese version of Social Strategies Rating Scale (SSRS). Administered to teachers, which rated on a 5-point scale (1=never, 3=half of the time, 5=almost always) how often the child uses the social strategies during interactions with peers on preschool context.
1 and 12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

January 2, 2022

Primary Completion (Actual)

June 9, 2022

Study Completion (Actual)

June 9, 2022

Study Registration Dates

First Submitted

December 28, 2022

First Submitted That Met QC Criteria

February 6, 2023

First Posted (Actual)

February 15, 2023

Study Record Updates

Last Update Posted (Actual)

February 17, 2023

Last Update Submitted That Met QC Criteria

February 15, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • BOICHI28122022

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

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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