- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07639437
Preprocedural Video Education for Bronchoscopy Anxiety
Preprocedural Video Education for Anxiety Reduction in Patients Undergoing Bronchoscopy Under General Anesthesia: A Randomized Clinical Trial
The goal of this clinical trial is to learn whether preprocedural video education can reduce anxiety in adult patients who are scheduled to undergo bronchoscopy under general anesthesia. It will compare video-based education with standard verbal education.
The main questions it aims to answer are:
Does video education reduce preprocedural anxiety, as measured by the Amsterdam Preoperative Anxiety and Information Scale (APAIS), in patients undergoing bronchoscopy under general anesthesia?
Researchers will compare patients who receive audiovisual education with those who receive standard verbal education to see whether video education provides greater anxiety reduction before bronchoscopy under general anesthesia.
Participants will:
- Complete an APAIS questionnaire before receiving preprocedural education
- Receive either video-based education using a tablet or standard verbal education with a question-and-answer session
- Complete another APAIS questionnaire immediately after the education session
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Jakarta Special Capital Region
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Jakarta, Jakarta Special Capital Region, Indonesia, 13230
- RSUP Persahabatan
-
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Adult patients aged ≥18 years who are scheduled to undergo bronchoscopy under general anesthesia.
- Patients with no previous history of medical procedures performed under general anesthesia.
- Patients with an American Society of Anesthesiologists (ASA) physical status classification of I-III.
- Patients who are willing to participate in the study and have provided written informed consent.
Exclusion Criteria:
- Patients who are unable to read and write.
- Patients with significant hearing and/or visual impairment.
- Patients with cognitive or mental disorders identified from the patient's medical record.
- Patients with a history of antipsychotic or benzodiazepine use.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: control group
Participants in the control group received standard preprocedural education through verbal explanation and a question-and-answer session delivered by the anesthesiologist.
The education was based on the standard anesthesia education materials used at RSUP Persahabatan.
APAIS scores were assessed before and immediately after the education session.
|
Participants received standard preprocedural education through verbal explanation and a question-and-answer session delivered by the anesthesiologist.
The education was based on the standard anesthesia education materials used at RSUP Persahabatan and provided information about bronchoscopy under general anesthesia.
The APAIS questionnaire was completed before and immediately after the verbal education session.
|
|
Sperimentale: intervention group
Participants in the intervention group received standard preprocedural verbal education and a question-and-answer session delivered by the anesthesiologist.
In addition, they received audiovisual education through a video presented on a tablet.
The video provided information about bronchoscopy under general anesthesia.
APAIS scores were assessed before and immediately after the education session.
|
Participants received standard preprocedural verbal education and a question-and-answer session delivered by the anesthesiologist.
In addition, participants watched an audiovisual educational video about bronchoscopy under general anesthesia on a tablet.
The video was designed to provide consistent information about the procedure and anesthesia process, improve patient understanding, and reduce preprocedural anxiety.
The APAIS questionnaire was completed before and immediately after the education session.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Pre-education total APAIS score
Lasso di tempo: single time point immediately before education
|
The pre-education total APAIS score was assessed before any educational intervention was delivered, using the Amsterdam Preoperative Anxiety and Information Scale (APAIS).
The APAIS consists of six items scored on a 5-point Likert scale, ranging from 1 ("not at all") to 5 ("extremely"), with higher total scores indicating greater preprocedural anxiety and information need.
|
single time point immediately before education
|
|
Post-education total APAIS score
Lasso di tempo: single time point immediately after education
|
The pre-education total APAIS score was assessed before any educational intervention was delivered, using the Amsterdam Preoperative Anxiety and Information Scale (APAIS).
The APAIS consists of six items scored on a 5-point Likert scale, ranging from 1 ("not at all") to 5 ("extremely"), with higher total scores indicating greater preprocedural anxiety and information need.
|
single time point immediately after education
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- 0045/KEPK-RSUPP/03/2025
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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