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QR Code-Based Video-Supported Anesthesia Information and Preoperative Anxiety (QR-AID)

9. juni 2026 opdateret af: Elazıg Fethi Sekin Sehir Hastanesi

The Effect of QR Code-Based Video-Supported Anesthesia Information on Preoperative Anxiety, Comprehensibility of Information, and Patient Satisfaction: A Prospective Randomized Controlled Study

This study aims to evaluate the effects of QR code-based video-supported anesthesia information on preoperative anxiety, comprehensibility of information, and patient satisfaction in adult patients undergoing elective surgery.

Participants will be randomly assigned in a 1:1 ratio to either a control group receiving standard written informed consent and routine verbal anesthesia information or an intervention group receiving the same standard information plus a standardized video-based educational intervention accessed through a QR code.

The primary outcome is the change in the Amsterdam Preoperative Anxiety and Information Scale (APAIS) anxiety score before and after the information process. Secondary outcomes include comprehensibility of information and patient satisfaction assessed using a structured Likert-type questionnaire.

The findings may contribute to the standardization of patient information processes in anesthesia outpatient clinics through a low-cost and easily implementable digital educational approach.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

Background:

Informed consent and patient information are essential components of perioperative care. However, written consent forms may be difficult for some patients to understand because of technical language, limited consultation time, and variations in verbal explanations provided by clinicians. Digital educational tools may improve patient understanding and reduce preoperative anxiety by providing standardized information.

Objective:

The primary objective of this randomized controlled trial is to determine whether QR code-based video-supported anesthesia information reduces preoperative anxiety compared with standard written and verbal information alone.

Methods:

This is a single-center, prospective, parallel-group randomized controlled trial conducted at Elazig Fethi Sekin City Hospital.

Adult patients scheduled for elective surgery will be screened for eligibility and randomized in a 1:1 ratio to either:

  1. Control Group:

    Standard written informed consent and routine verbal anesthesia information.

  2. Intervention Group:

Standard written informed consent and routine verbal anesthesia information plus a standardized video-based educational intervention delivered through a QR code and viewed using a tablet device and headphones.

The educational video includes information regarding:

  • Purpose of anesthesia
  • Types of anesthesia
  • Preoperative fasting requirements
  • Preparation for surgery
  • Perioperative process
  • Potential complications
  • Common temporary side effects
  • Patient rights
  • Meaning and importance of informed consent

Outcomes:

Primary Outcome:

Change in Amsterdam Preoperative Anxiety and Information Scale (APAIS) anxiety score measured before and after completion of the information process.

Secondary Outcomes:

  • Comprehensibility of information
  • Patient satisfaction

Both secondary outcomes will be assessed using a structured 10-item Likert-type questionnaire.

Expected Impact:

This study will evaluate whether a standardized QR code-based video education model can improve patient understanding, reduce anxiety, and increase satisfaction. If effective, the intervention may provide a scalable and low-cost strategy for standardizing anesthesia information processes in routine clinical practice.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

284

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

  • Tyrkiet (Türkiye)
    • Elâzığ
      • Elâzığ, Elâzığ, Tyrkiet (Türkiye), 23100
        • Elazığ Fethi Sekin City Hospital
        • Ledende efterforsker:
          • Sevim Şenol Karataş, MD
        • Kontakt:
        • Kontakt:
        • Underforsker:
          • Sait F Öner, MD
        • Underforsker:
          • Ferhat Karataş, PhD Student

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Age 18 years or older
  • Scheduled for elective surgery
  • Evaluated in the anesthesia outpatient clinic
  • Able to understand the study information and questionnaires
  • Able to provide written informed consent

Exclusion Criteria:

  • Emergency surgery
  • Impaired consciousness
  • Advanced dementia
  • Severe psychiatric illness
  • Severe visual, hearing, or cognitive impairment
  • Inability to understand the digital educational content
  • Refusal to participate
  • Inability to read or understand Turkish

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Control Group
Participants receive standard written informed consent and routine verbal anesthesia information according to routine clinical practice.
Eksperimentel: QR Video Group
Participants receive standard written informed consent and routine verbal anesthesia information plus a standardized QR code-based video-supported anesthesia education program.
Adfærdsmæssigt: QR Code-Based Video-Supported Anesthesia Information
Participants receive standard written informed consent and routine verbal anesthesia information plus a standardized QR code-based video-supported educational intervention. The video includes information regarding anesthesia types, fasting requirements, perioperative preparation, potential complications, common side effects, patient rights, and informed consent.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in APAIS Anxiety Score
Tidsramme: Immediately before and immediately after completion of the information process (same study visit)
Change in the Amsterdam Preoperative Anxiety and Information Scale (APAIS) anxiety subscale score from before the information process (T1) to after completion of the information process (T2).
Immediately before and immediately after completion of the information process (same study visit)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Information Comprehensibility Score
Tidsramme: Immediately after completion of the information process
Comprehensibility of anesthesia information assessed using a structured 10-item Likert-type questionnaire.
Immediately after completion of the information process
Patient Satisfaction Score
Tidsramme: Immediately after completion of the information process
Patient satisfaction with the anesthesia information process assessed using a structured 10-item Likert-type questionnaire.
Immediately after completion of the information process

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Elazıg Fethi Sekin Sehir Hastanesi

Efterforskere

  • Ledende efterforsker: Sevim Şenol Karataş, Elazıg Fethi Sekin Sehir Hastanesi

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

10. juni 2026

Primær færdiggørelse (Anslået)

10. juli 2026

Studieafslutning (Anslået)

10. juli 2026

Datoer for studieregistrering

Først indsendt

9. juni 2026

Først indsendt, der opfyldte QC-kriterier

9. juni 2026

Først opslået (Faktiske)

15. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

15. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • QR Code-Based Video

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

IPD-planbeskrivelse

Individual participant data will not be made publicly available because the study involves patient-level clinical information and no data-sharing plan has been established at the time of registration.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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