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Role of Preoperative Counselling With NSQIP Surgical Risk Calculator

Role of Preoperative Counselling With NSQIP Surgical Risk Calculator

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04757402
Enrollment
66
Registered
2021-02-17
Start date
2021-04-01
Completion date
2023-10-28
Last updated
2023-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Satisfaction, Patient

Keywords

NSQIP Surgical risk calculator, Preoperative counselling, Anxiety

Brief summary

Surgical patients undergo preoperative counseling which varies in quality and duration. Proper communication during the preoperative consultation can deliver relevant health information and guide improvement of perioperative health status. The methods, however, are non-standardized and the explanation of the postoperative course is generally vague or varies from person to person. We hypothesize that high-risk patients who receive pre-operative counseling with the help of the NSQIP surgical risk calculator compared to the current standard of care will have higher satisfaction concerning information on the perioperative journey.

Detailed description

The control arm will receive standard preoperative counselling and written consent will be taken. The NSQIP arm will receive standard preoperative counselling along with the details provided by NSQIP Surgical risk calculator and written consent will be taken. Anxiety among the patients will be accessed with the use of Preoperative anxiety measured by Amsterdam Preoperative Anxiety and Information Scale (APAIS) questionnaire written in Nepali. Duration of counselling period will be noted from the start of counselling session till the consent is signed.

Interventions

OTHERCounselling with NSQIP Surgical risk calculator

Use of NSQIP surgical risk calculator to check for patient satisfaction regarding pre operative counseling.

Sponsors

Nepal Mediciti Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ASA III or above and/or age above 65 high-risk surgical patients undergoing surgery at Nepal Mediciti Hospital

Exclusion criteria

* Adults who cannot consent Pregnant women Non-Nepali speakers Consent by surrogate

Design outcomes

Primary

MeasureTime frameDescription
The difference in patient satisfaction as assessed by a 7-point Likert scale5 MONTHSThe study will compare patient satisfaction scores between the two arms of the study groups to determine if there is a difference in patient satisfaction. It will be based on a scale of 1 to 7, 7 being the most satisfied and 1 being the least.

Secondary

MeasureTime frameDescription
Preoperative anxiety measured by Amsterdam Preoperative Anxiety and Information Scale (APAIS) questionnaire written in Nepalese5 monthsAnxiety evaluation during preoperative counselling will be done by APAIS using a five point scale,5 being the most anxious and 1 being the least.
Duration of counseling5 monthstime taken to complete preoperative counseling which will be noted from start of counseling to the time when consent is signed.

Countries

Nepal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026