Pain Neuroscience Education for Middle School Students

Kutahya Health Sciences University

Status

Not yet enrolling

Conditions

Neuroscience Pain Education

Physical Activity

Pediatrics

Pain

Treatments

Other: Turkish PNE4Kids

Study type

Interventional

Funder types

Other

Identifiers

NCT06869369

Turkish PNE4Kids

Details and patient eligibility

About

This project was designed as a single-blind, randomised controlled, prospective intervention study. The research question of the project is 'Is pain neuroscience education an effective method to improve various aspects of child health, conceptualise pain and change pain-related behaviours in middle school children?'. In other words, the aim of this project is to investigate whether pain neuroscience education (PNE4Kids) is an effective method for improving various aspects of child health, conceptualising pain and changing pain-related behaviours in middle school children. For this purpose, it is planned to implement PNE4Kids based power point presentation and interactive game training. It is aimed to evaluate children in terms of physical activity level, sleep quality/habits, pain conceptualisation level and participation in leisure time activities. Physical activity levels will be assessed with Actigraph GT3X+ accelerometer device and 'Physical Activity Scale for Older Children'. Sleep quality/ habits will be assessed with Actigraph GT3X+ accelerometer and 'Children's Sleep Habits Scale-short form'. Knowledge of pain conceptualisation will be assessed with the 'Conceptualisation of Pain' scale. Children's level of participation in leisure time activities will be assessed through the participation section/domain of the Participation Environment Measure for Children and Youth (PEM-CY). After the baseline measurements of the individuals included in the study and who volunteered will be completed, they will be randomly assigned to the control or intervention group. Participants in the intervention group will receive 'Turkish PNE4Kids Programme'. Individuals in the control group will not receive any intervention. All evaluations will be repeated before the training, immediately after the training and at the end of the 3rd month after the training.

Enrollment

57 estimated patients

Sex

All

Ages

10 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Being actively educated at midschool level,
Having sufficient reading and understanding skills in Turkish.

Exclusion criteria

Chronic pain (pain in ≥1 anatomic region that persists or recurs for longer than 3 months,
Chronic illness (e.g. cancer, diabetes, asthma, juvenile rheumatic arthritis),
Being diagnosed with a specific learning disability,
Being diagnosed with attention deficit hyperactivity disorder,
Being diagnosed with autism spectrum disorder,
Not being willing to participate in the study by oneself or one's parents.