- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05870085
Impact of Neuro-linguistic Programming on Schoolchildren's Performance
Impact of Neuro-linguistic Programs on the Academic Performance of Primary School Students in Lebanon: Triggers, Attention Deficit Hyperactivity Disorder Symptoms and Their Effect on Behavior and Academic Performance of Schoolchildren
Neuro-Linguistic Programming (NLP) is a methodology developed in the 1970s by Richard Bandler and John Grinder, based on the idea that language and behavior are interconnected and can be systematically modeled and changed. NLP is often used as a form of psychotherapy, coaching, or personal development, although its effectiveness has been debated in the scientific community.
NLP practitioners believe that our thoughts, emotions, and behavior are influenced by our internal representations of the world, which are constructed through language and sensory experiences. Changing the use of language and the perception of experiences, thoughts, emotions, and behavior can be adjusted accordingly. NLP uses various techniques to achieve this, including reframing, anchoring, and rapport-building. Reframing involves changing the perception of a situation by putting it in a different context or perspective. Anchoring consists in associating a particular state of mind or emotion with a specific physical or sensory stimulus, such as a touch or a smell. Rapport-building involves establishing a connection and a sense of trust with another person through mirroring and matching their body language, tone of voice, and language patterns.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Beirut, Lebanon
- Notre dame de la paix
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Schoolchildren aged between 5 and 11 years attending the same school for at least a year.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Triple
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Identification of school triggers through ''Identify School Triggers'' questionnaire
Time Frame: 2 months after the intervention
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130 children will be asked to fill out the ''Identify school triggers'' questionnaire by rating items depending on the strength of the trigger impact.
A score over 20 will be calculated and the strength of the triggers will be evaluated after categorizing the scores.
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2 months after the intervention
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Schoolchildren's strengths and difficulties progression through the Strengths and Difficulties Questionnaire
Time Frame: 2 months after the intervention
|
A parent (mother or father or legal guardian) of 130 children will be asked to fill out a survey.
The first 25 items in the SDQ comprise 5 scales of 5 items each.
It is usually easiest to score all 5 scales before working out the Total Difficulties score.
Somewhat True is always scored as 1, but the scoring of Not True and Certainly True varies with each item.
For each of the 5 scales, the score can range from 0-10 if all 5 items were completed.
Scale scores can be prorated if at least 3 items were completed.
Using the comments, a "substantial risk of clinically significant problems" score on the Total Difficulties Score can be used to identify likely ''cases" with mental disorders.
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2 months after the intervention
|
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Concentration, hyperactivity, and reasoning of schoolchildren through the Vanderbilt Assessment Scale
Time Frame: 2 months after the intervention
|
Two different teachers will complete the survey for each student (130 students and 12 teachers). The initial assessment scales, parent and teacher, have two components: Symptom assessment and impairment in performance. Symptom assessment screens for symptoms that meet the criteria for inattentive (items 1-9) and hyperactive attention deficit hyperactivity disorder (ADHD) (items 10-18). To meet the requirements for the diagnosis, one must have at least six positive responses to either the inattentive nine or hyperactive nine core symptoms, or both. The specific item sets and numbers of positives required for each co-morbid symptom screen set are detailed below. The second section of the scale has many performance measures, scored 1 to 5, with 4 and 5 being somewhat of a problem/problematic. |
2 months after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Roula Abou Assi, PhD, Lebanese University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3/23/D
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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