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Effects of Different Transport Methods on Preoperative Anxiety and Fear in Preschool Children

10 augusti 2026 uppdaterad av: İlayda Tekelioğlu, Ege University
Preoperative anxiety and fear are common among preschool children undergoing surgery and may negatively affect perioperative cooperation and postoperative recovery. This study aims to evaluate the effects of three different operating room transport methods (walking with a parent, stretcher transport, and battery-powered ride-on car transport) on preoperative anxiety and fear levels in preschool children undergoing day surgery. The findings are expected to contribute to the development of child-friendly, non-pharmacological interventions to improve the perioperative experience of children.

Studieöversikt

Detaljerad beskrivning

Preoperative anxiety is frequently observed in preschool children undergoing surgical procedures. The unfamiliar hospital environment, separation from parents, and fear of anesthesia and surgery may increase children's anxiety and fear before surgery. Elevated preoperative anxiety has been associated with poor cooperation during anesthesia induction, increased postoperative pain, maladaptive behavioral changes, and delayed recovery.

Several non-pharmacological interventions have been developed to reduce children's anxiety before surgery. Among these, distraction techniques and child-friendly environmental modifications have shown promising results. Transporting children to the operating room using battery-powered ride-on cars has recently emerged as an innovative distraction strategy that may transform the transport process into a playful experience.

This controlled study aims to compare three different operating room transport methods in preschool children undergoing elective day surgery: routine transport by walking with a parent, transport by stretcher, and transport using a battery-powered ride-on car. Preoperative anxiety and fear will be assessed using validated pediatric assessment tools before surgery. The study findings may provide evidence for the effectiveness of child-friendly transport methods in reducing preoperative anxiety and fear and support the implementation of non-pharmacological interventions in pediatric surgical care.

Studietyp

Interventionell

Inskrivning (Beräknad)

66

Fas

  • Inte tillämpbar

Kontakter och platser

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Studiekontakt

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  • Children aged 3-6 years (36-72 months)
  • Scheduled to undergo elective surgery in the Department of Pediatric Surgery
  • Able to communicate appropriately for their age
  • Have sufficient cognitive development to respond to the study assessment scales
  • Child and parent/legal guardian are able to speak and understand Turkish
  • Written informed consent obtained from the child's legal guardian (and child assent obtained when appropriate)

Exclusion Criteria:

  • Presence of visual, hearing, or communication impairments that could interfere with study participation
  • Receipt of premedication requiring sedation due to an emergency condition
  • Presence of severe pain that could affect anxiety assessment before surgery
  • Inability to safely use the battery-powered ride-on car because of physical or mobility limitations before surgery
  • Withdrawal of consent by the child's legal guardian or the child's unwillingness to continue participation

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: Routine Walking with Parent
Participants are transported to the operating room by walking with a parent according to the hospital's routine practice.
Participants are transported to the operating room by walking with a parent according to the hospital's routine practice.
Experimentell: Stretcher Transport
Participants are transported to the operating room using a stretcher.
Participants are transported to the operating room using a stretcher.
Experimentell: Battery-Powered Ride-on Car Transport
Participants are transported to the operating room using an age-appropriate battery-powered ride-on car accompanied by the researcher.
Participants are transported to the operating room using an age-appropriate battery-powered ride-on car accompanied by the researcher.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Preoperative Anxiety Level
Tidsram: Immediately before transfer to the operating room (preoperative period).
Preoperative anxiety levels will be assessed using the Children's Anxiety Scale-State (CAS-S), a visual thermometer-like scale with scores ranging from 0 to 10. Higher scores indicate higher levels of state anxiety. Scores will be compared among preschool children transported to the operating room by walking with a parent, stretcher, or battery-powered ride-on car.
Immediately before transfer to the operating room (preoperative period).

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Preoperative Fear Level
Tidsram: Immediately before transfer to the operating room (preoperative period)
Preoperative fear levels will be assessed using the Children's Fear Scale (CFS), which consists of five facial expressions and is scored from 0 to 4. A score of 0 indicates no fear, while a score of 4 indicates severe fear. Higher scores indicate higher levels of fear. Scores will be compared among preschool children transported to the operating room by walking with a parent, stretcher, or battery-powered ride-on car.
Immediately before transfer to the operating room (preoperative period)

Samarbetspartners och utredare

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Sponsor

Utredare

  • Huvudutredare: Nurdan Akçay Didişen, PhD, Ege university

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

31 juli 2026

Primärt slutförande (Beräknad)

31 juli 2027

Avslutad studie (Beräknad)

31 juli 2027

Studieregistreringsdatum

Först inskickad

26 juli 2026

Först inskickad som uppfyllde QC-kriterierna

26 juli 2026

Första postat (Faktisk)

30 juli 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

12 augusti 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

10 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

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Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

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Studerar en amerikansk FDA-reglerad produktprodukt

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