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Fear and Anxiety in Anesthesia-Naïve Patients Pre-operatively vs Post-operatively

29. april 2026 oppdatert av: Ana Costa, Stony Brook University

Fear and Anesthesia: How Anxiety and Fear in Anesthesia-Naïve Patients Changes From Preop to Postop

The goal of this observational study is to understand how fear and anxiety felt by anesthesia-naive patients compares before versus after their scheduled surgery. Patients who are scheduled to undergo a low-risk surgery/procedure and have never had anesthesia before will be asked to:

Fill out a survey before their surgery in the perioperative setting
Answer follow-up questions over the phone a few days after their surgery.

Studieoversikt

Status

Rekruttering

Forhold

Intervensjon / Behandling

Annen: Survey using a questionnaire.

Detaljert beskrivelse

Patients that fit the inclusion/exclusion criteria and consent to the study will fill out a paper survey that is an adapted version of the Amsterdam Preoperative Anxiety and Information Scale (APAIS) along with additional questions related to anesthesia anxiety for secondary analysis. 7 days (+/-72 hours) after the patient's surgery, they will complete a follow-up survey over the phone that is an adapted version of the APAIS. Results will be recorded on paper and then uploaded into REDCap for data analysis.

Studietype

Observasjonsmessig

Registrering (Antatt)

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Navn: Anna Suske
Telefonnummer: 631-638-1214
E-post: anna.suske@stonybrookmedicine.edu

Studiesteder

Forente stater
- New York
  - Stony Brook, New York, Forente stater, 11794
    - Rekruttering
    - Stony Brook University Hospital
    - Ta kontakt med:
      
      Anna Suske
      
      Telefonnummer: 631-638-1214
      
      E-post: anna.suske@stonybrookmedicine.edu
    - Ta kontakt med:
      
      Ana Costa, MD
      
      Telefonnummer: 631-358-6513
      
      E-post: ana.costa@stonybrookmedicine.edu
    - Hovedetterforsker:
      
      Ana Costa, MD

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

Voksen
Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Patients over 18 who have never received anesthesia before that are scheduled to undergo a low-risk surgery/procedure at Stony Brook University Hospital, Stony Brook Ambulatory Surgery Center, or Stony Brook Ambulatory Care Pavilion.

Beskrivelse

Inclusion Criteria:

18 years old or over
Patients scheduled to undergo surgeries such as but not limited to:

cholecystectomies, appendectomies, hernia repairs, breast surgeries, plastic surgeries, thyroidectomy, parathyroidectomy, tonsillectomy, adenoidectomy, lithotripsy, stent placement, kidney stone surgeries, cystoscopies, bladder tumors, ovarian cystectomies, hysterectomies, tubal ligation, hysteroscopy, Intrauterine Device (IUD) insertion, knee replacement, hip replacement, fracture pinning, sports injury surgery such as knee and shoulder scopes. OR patients undergoing procedures such as but not limited to: colonoscopies and endoscopies

Patient undergoing anesthesia for the first time
Patients who are not pregnant by self report

Exclusion Criteria:

Patients under 18
Patients who are pregnant
Patients undergoing high-risk surgeries
Patients undergoing cancer-related procedures
Non-English speaking patients
Patients that experience mental status change postoperatively as determined by the medical teams caring for the patient
Patients with an existing anxiety disorder, or psychiatric diagnoses
Patients on benzodiazepines, antidepressants, chronic opioids

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Hva måler studien?

Primære resultatmål

Resultatmål	Tiltaksbeskrivelse	Tidsramme
Differences in anxiety scale scores pre- and post-operatively in anesthesia-naïve patients Tidsramme: From enrollment until 7 days (+/-72 hours) post-operative	Participants will be given 2 scores based on their pre-operative survey and their post-operative survey. The change in anxiety score will be evaluated.	From enrollment until 7 days (+/-72 hours) post-operative

Sekundære resultatmål

Resultatmål	Tiltaksbeskrivelse	Tidsramme
Determining if there is an association between a pre-operative desire for information related to anesthesia and the post-operative reality of the individual subject's anesthesia experience. Tidsramme: From enrollment until 7 days (+/-71 hours) post-operative	This data will be collected from the pre-operative and post-operative survey questionnaires and evaluated for correlation.	From enrollment until 7 days (+/-71 hours) post-operative
Comparing the frequency of specific fears of events pre-operatively versus the post-operative reality of the individual subject's anesthesia experience. Tidsramme: From enrollment until 7 days (+/-71 hours) post-operative	This data will be collected from the pre-operative and post-operative survey questionnaires and will be evaluated.	From enrollment until 7 days (+/-71 hours) post-operative

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Stony Brook University

Etterforskere

Hovedetterforsker: Ana Costa, MD, Stony Brook University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

12. februar 2026

Primær fullføring (Antatt)

1. februar 2027

Studiet fullført (Antatt)

1. februar 2027

Datoer for studieregistrering

Først innsendt

23. april 2026

Først innsendt som oppfylte QC-kriteriene