Effects of Rainbow Parachute Games on UE Strength and Social-Emotional Skills in Children With Developmental Delay
10 agosto 2026 aggiornato da: Riphah International University
Effects of Rainbow Parachute Games on Upper Extremity Strength and Social-Emotional Skills in Children With Developmental Delay
Conducted as a randomized trial, this study examines the impact of rainbow parachute games on upper extremity strength and social-emotional skills in children (ages 5-8) with developmental delays.
Participants will be randomly divided experimental and control groups.
The experimental group performs parachute activities for 8 weeks, while the control group does rhyming activities.
Outcomes measured by "Hand held Dynamometer" and "Pediatric Arm Function Test (PAFT)" for upper extremity strength and Social-Emotional skills will be measured by "Strengths and Difficulties Questionnaire (SDQ)".
Statistical analysis will be performed using SPSS version 2023 to determine the Intervention's effects.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Children with developmental delay often experience challenges in Physical and Social-emotional domains, which can affect their overall growth and daily functioning. Addressing these deficits early through engaging and structured interventions is essential for promoting developmental progress and enhancing quality of life. The aim of this study is to investigate the effect of Rainbow Parachute Games on Upper Extremity Strength and Social-Emotional Skills in children with developmental delay.
The study design will be a Randomized controlled trial.12children age ranged from 5-8years with developmental delays will be randomly assigned either into an experimental group (n=6) or control group (n=6). The intervention "Rainbow parachute games" will be performed for 8 weeks (3 sessions/week). Each session will take 35-40min. Control group includes Rhyming activities, duration for control group activity will be 20min. All the referred participants will be assessed for the eligibility criteria. Guardians of participants will be asked to sign the consent forms before entering them to the study. Upper Extremity Strength will be measured by "Hand held Dynamometer" and "Pediatric Arm Function Test (PAFT)". Social-Emotional skills will be measured by "Strengths and Difficulties Questionnaire (SDQ)".
Tipo di studio
Interventistico
Iscrizione (Effettivo)
12
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Riphah International University
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Bambino
Accetta volontari sani
No
Descrizione
Inclusion Criteria:
- Children aged 5-8 years.
- Diagnosed with motor developmental Delay.
- Both Girls and Boys will be Included.
Exclusion Criteria:
- Severe Physical Disability.
- Uncontrolled medical Health conditions that contraindicate Physical activity.
- Severe Visual or Auditory impairments that limit engagement in group activities.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Group A : Intervention Group (Rainbow parachute Games and Rhyming Activities)
The participants in this group will receive both the Rhyming activities and Rainbow parachute game activities.
Rhyming activities will be performed first, participants will clap or make patterns with hands in air on the words that rhyme, once they're already familiar with the text (Little mouse, The bird), directions will be given and shown how to wave and make patterns with variations and rhythm these activities will be performed for 20 min.
After Rhyming activities, Parachute activities will be performed in 25-30min.
Intervention will be given for 8 weeks (3 sessions/week).
Each session will take 45-50 mins.
The intervention consists of different play activities with Rainbow parachute
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Group A : The participants in this group will receive both the Rhyming activities and Rainbow parachute game activities.
Rhyming activities will be performed first, participants will clap or make patterns with hands in air on the words that rhyme, once they're already familiar with the text (Little mouse, The bird), directions will be given and shown how to wave and make patterns with variations and rhythm these activities will be performed for 20 min.
After Rhyming activities, Parachute activities will be performed in 25-30min.
Intervention will be given for 8 weeks (3 sessions/week).
Each session will take 45-50 mins.
The intervention consists of different play activities with Rainbow parachute.
Activities like Make waves, Treasure under the sea, Mushroom, Cat and mouse, Paracute Tug will be performed and pre and post results will be analysed
Altri nomi:
Group B : Participants in the control group will perform Rhyming activities participants will clap or make patterns with hands in air on the words that rhyme, once they're already familiar with the text (Little mouse, The bird), directions will be given and shown how to wave and make patterns with variations and rhythm these activities will be performed for 20 mins.
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Sperimentale: Group B: Control Group (Rhyming Activities)
Participants in the control group will perform Rhyming activities participants will clap or make patterns with hands in air on the words that rhyme, once they're already familiar with the text (Little mouse, The bird), directions will be given and shown how to wave and make patterns with variations and rhythm these activities will be performed for 20 mins
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Group B : Participants in the control group will perform Rhyming activities participants will clap or make patterns with hands in air on the words that rhyme, once they're already familiar with the text (Little mouse, The bird), directions will be given and shown how to wave and make patterns with variations and rhythm these activities will be performed for 20 mins.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Social-Emotional skills by Strengths and Difficulties Questionnaire
Lasso di tempo: 8 weeks
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Social-Emotional skills will be measured by "Strengths and Difficulties Questionnaire (SDQ)".
The Strengths and Difficulties Questionnaire (SDQ) is a 25-item behavioral screening tool for children and young people aged 2 to 17.
It uses a 3-point response scale ("Not True," "Somewhat True," and "Certainly True") mapped across five subscales, a Total Difficulties score, and an Impact score
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8 weeks
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Upper Extremity Strength by Pediatric Arm Function Test
Lasso di tempo: 8 weeks
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Pediatric Arm Function Test (PAFT) will be used to access upper extremity strength, The Pediatric Arm Function Test (PAFT) is scored by trained occupational therapists who evaluate video recordings of a child (typically ages 2 to 12 with hemiparesis) completing specific functional and play tasks.
It uses two primary sub-scales: the Functional Ability scale (rating movement quality/execution of the more-affected arm) and the Limb Preference scale (calculating the percentage of tasks spontaneously attempted with that arm)
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8 weeks
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Arooj Abid, MS-PPT, Riphah International University
Pubblicazioni e link utili
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Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
28 ottobre 2025
Completamento primario (Effettivo)
25 giugno 2026
Completamento dello studio (Effettivo)
15 luglio 2026
Date di iscrizione allo studio
Primo inviato
27 luglio 2026
Primo inviato che soddisfa i criteri di controllo qualità
10 agosto 2026
Primo Inserito (Effettivo)
11 agosto 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
11 agosto 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
10 agosto 2026
Ultimo verificato
1 agosto 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- REC/RCR&AHS/25/0703
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
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