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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorStony Brook University

About this trial

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:

1. Fill out a survey before their surgery in the perioperative setting 2. Answer follow-up questions over the phone a few days after their surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18 years old or over

Patient undergoing anesthesia for the first time

Patients who are not pregnant by self report

Disqualifiers

Patients under 18

Patients who are pregnant

Patients undergoing high-risk surgeries

Patients undergoing cancer-related procedures

Trial population

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.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Survey using a questionnaire.

    Other intervention

    A preoperative and postoperative survey questionnaire that is adapted from the Amsterdam Preoperative Anxiety and Information Scale and includes additional questions regarding their anesthesia and operative care.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Differences in anxiety scale scores pre- and post-operatively in anesthesia-naïve patients

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.

Time frame
From enrollment until 7 days (+/-72 hours) post-operative

Secondary outcomes

1

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.

This data will be collected from the pre-operative and post-operative survey questionnaires and evaluated for correlation.

Time frame
From enrollment until 7 days (+/-71 hours) post-operative
2

Comparing the frequency of specific fears of events pre-operatively versus the post-operative reality of the individual subject's anesthesia experience.

This data will be collected from the pre-operative and post-operative survey questionnaires and will be evaluated.

Time frame
From enrollment until 7 days (+/-71 hours) post-operative

Other outcomes

Sponsors and contacts

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