To Develop a Validated Program and Use it to Evaluate Patients Post-operatively

NCT03037996 | Unknown DMC

• 1 other identifier: COA no. Si 790/2016
• Study Type: observational
• Target: 450
• Locations: 1 country
• Sites: 2

Brief Summary

Annually, the Department of Anesthesiology, Siriraj hospital has responsibilities to take care of more than 50,000 patients peri-operatively. According to Maslow's hierarchy of needs; human's pleasure is classified as physiological, safety, belonging, esteem and self-actualization. Since defining and measuring quality of healthcare service is an inevitable challenge for all institutes in medical fields, a questionnaire is developed to assess the quality of all services. The Siriraj Anesthesia Quality Assessment Questionnaire (Si-2-AQ), a simply 40-item tool in seven dimensions, comprises Accessibility and convenience, Communication and Information, Process of care, Technical Quality, Psychological support, Physical support and Royalty.

Conditions

Patient Relations, Nurse; Post-operative Patients

Keywords

anesthesia; satisfaction

Outcome Measures

Primary Outcomes (1)

• Patients' satisfaction

  questionnaires

  4 months

Interventions

patients' response OTHER

patients' satisfaction to anesthesia services

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

A developed and validated questionnaire will be studied in 450 patients as target group (4 months). Post-operatively, a nurse anesthetist visits a patient to explain the details of the study and ask for consent. Afterwards, a participant responses to a questionnaire privately (10 minutes). Co-investigators collect data in a computer file. A statistician who not involved in the study analyzes the data.

You may qualify if:

• Volunteered, literate and communicable, well-conscious, in-patients ASA I-III, aged 18-65 years who underwent elective surgery.

You may not qualify if:

• Patients with severe diseases such as congestive heart failure, end-stage renal disease, etc. Patients refuse to join the study.

Sponsors & Collaborators

• Siriraj Hospital: lead

Study Sites (2)

Faculty of Medicine Siriraj Hospital, Mahidol University

Bangkok Noi, Bangkok, 10700, Thailand

Location

Faculty of Medicine Siriraj Hospital, Mahidol University

Bangkoknoi, Bangkok, 10700, Thailand

Location

MeSH Terms

Conditions

Personal Satisfaction

Condition Hierarchy (Ancestors)

Behavior

Study Officials

• Chairal Shayakul, M.D.

  Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand

  STUDY CHAIR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 4 Months
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: January 23, 2017
• First Posted: January 31, 2017
• Study Start: January 23, 2017
• Primary Completion: December 31, 2017
• Study Completion: December 31, 2017
• Last Updated: October 6, 2017

Record last verified: 2017-10

Data Sharing

• IPD Sharing: Will not share

Locations

TH (2)