The Effect of Animation Therapy on Time Perception in Primary School Children: A Randomized Controlled Study

Sponsor
Kutahya Health Sciences University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05898490
Collaborator
(none)
60
1
2
5.1
11.7

Study Details

Study Description

Brief Summary

The aim of the study is to determine the effects of animation therapy on time perception and daily activity routine performances of primary school children.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Animation Therapy
N/A

Detailed Description

Time is a process that forms the basis of executive functions used to reveal adaptive behavior and motor performance. However, the way we perceive time can be changed by different factors. This may reveal changes in executive functions such as decision making, behavioral inhibition, planning, and accordingly, in the performance levels and daily routines of daily living activities. Animation therapy is the therapeutic use of the process of shooting a stop-motion animation film. It creates a "flow" effect by nature. The concept of flow includes the loss of the sense of time. In this study, it is aimed to examine whether animation therapy has an effect on the perception of time and daily activity routines in primary school children.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effect of Animation Therapy on Time Perception in Primary School Children: A Randomized Controlled Study
Actual Study Start Date :
May 29, 2023
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Animation Therapy Group

10 sessions of Animation Therapy (2 session/week)

Behavioral: Animation Therapy
The process of shooting a stop-motion animation film, is designed according to the interests and leading of the participant.

No Intervention: Control Froup

No intervention

Outcome Measures

Primary Outcome Measures

  1. Time Discrimination Task [Baseline, preintervention]

    Time Discrimination Task is based on the individual's perception of the time difference of two different gaps between two pairs of sequentially given stimuli. Generally, the person is asked to indicate which pair is longer or shorter between two pairs of stimuli of certain lengths, which are given visually and/or audibly. Leveling is performed with the UDTR (Up-Down Transformed-Response) adaptive procedure method to progress the test and determine the participant's discrimination threshold.

  2. Time Discrimination Task [Immediately after the intervention]

    Time Discrimination Task is based on the individual's perception of the time difference of two different gaps between two pairs of sequentially given stimuli. Generally, the person is asked to indicate which pair is longer or shorter between two pairs of stimuli of certain lengths, which are given visually and/or audibly. Leveling is performed with the UDTR (Up-Down Transformed-Response) adaptive procedure method to progress the test and determine the participant's discrimination threshold.

  3. Time Reproduction Task [Baseline, preintervention]

    In Time Reproduction Task, the participants are asked to produce a stimulus similar to the duration of the stimulus presented to them at certain durations. In our study, visual and auditory stimuli of 200ms, 500ms and 800ms will be presented to the person in the time reproduction task, as in the time discrimination task. These stimuli will be presented in a completely random order, not in a specific order, and each stimulus will be presented 10 times, with a total of 30 consecutive stimuli. A gap of 2000 ms will be left between both stimuli to allow enough time for the person to reproduce the stimulus. The ratio of the absolute value of the difference between the participant's reproduced time and the target time to the target time will be calculated.

  4. Time Reproduction Task [Immediately after the intervention]

    In Time Reproduction Task, the participants are asked to produce a stimulus similar to the duration of the stimulus presented to them at certain durations. In our study, visual and auditory stimuli of 200ms, 500ms and 800ms will be presented to the person in the time reproduction task, as in the time discrimination task. These stimuli will be presented in a completely random order, not in a specific order, and each stimulus will be presented 10 times, with a total of 30 consecutive stimuli. A gap of 2000 ms will be left between both stimuli to allow enough time for the person to reproduce the stimulus. The ratio of the absolute value of the difference between the participant's reproduced time and the target time to the target time will be calculated.

  5. Executive Functions and Occupational Routines Score [Baseline, preintervention]

    This scale evaluates children's performance in daily activity routines, was developed by Fisch and Rosenblum in 2014. This scale evaluates the daily routines and executive functions of children aged 6-12 years, according to the opinion of their parents/caregivers. It consists of 3 sub-dimensions: Morning and Evening Routines (16 items), Game and Leisure Routines (7 items), and Social Routines (7 items). It is in the form of a five-point Likert scale and each item can be scored between 1 (never) and 5 (always). A high score indicates that the child's performance is high. The scale, which consists of 30 items in total, can be completed in approximately 15 minutes.

  6. Executive Functions and Occupational Routines Score [Immediately after the intervention]

    This scale evaluates children's performance in daily activity routines, was developed by Fisch and Rosenblum in 2014. This scale evaluates the daily routines and executive functions of children aged 6-12 years, according to the opinion of their parents/caregivers. It consists of 3 sub-dimensions: Morning and Evening Routines (16 items), Game and Leisure Routines (7 items), and Social Routines (7 items). It is in the form of a five-point Likert scale and each item can be scored between 1 (never) and 5 (always). A high score indicates that the child's performance is high. The scale, which consists of 30 items in total, can be completed in approximately 15 minutes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Being between the ages of 7-10

  • Absence of any orthopedic, neurodevelopmental, and psychiatric problems/diagnosis

  • Continuing formal education

  • Voluntarily agreeing to participate in the research

Exclusion Criteria:
  • Receiving orthopedic, neurodevelopmental and psychiatric diagnosis during the study period

  • To be absent from the study process or to quit the process

  • Not participating in the first and last evaluations

  • Voluntary refusal to participate or continue with the research

Contacts and Locations

Locations

Site City State Country Postal Code
1 Özel Yaşam Köyü İlkokulu Eskişehir Turkey

Sponsors and Collaborators

  • Kutahya Health Sciences University

Investigators

  • Study Director: Gonca Bumin, Prof., Hacettepe University
  • Principal Investigator: Özgün Belen, MSc, Kütahya Health Sciences University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ozgun Belen, Principal Investigator, Kutahya Health Sciences University
ClinicalTrials.gov Identifier:
NCT05898490
Other Study ID Numbers:
  • 2023-03/06
First Posted:
Jun 12, 2023
Last Update Posted:
Jun 12, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ozgun Belen, Principal Investigator, Kutahya Health Sciences University

Study Results

No Results Posted as of Jun 12, 2023