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Preoperative Risk Assessment in the Elderly

Web-based Preoperative Risk Assessment in the Elderly: a Pilot-study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04160234
Acronym
PrepTAB
Enrollment
100
Registered
2019-11-12
Start date
2019-11-22
Completion date
2022-01-31
Last updated
2021-02-10

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

Conditions

Preoperative Risk Assessment

Keywords

elderly, surgery, preoperative risk

Brief summary

PrepTAB aims to determine whether elderly patients are able to complete 4 preoperative risk assessment questionnaires within a web-based survey.

Detailed description

Elderly patients are the most rapidly increasing group among surgical admissions. They are prone to a higher risk, because of predisposing risk factors. A comprehensive preoperative risk assessment is recommended by the European Society of Anaesthesiologists guideline, but time-consuming and usually not performed at present. A telemedical approach would enable an out-of hospital risk assessment before hospital admission and provide important information without the need for additional in-hospital resources. The feasibility of the completion of a web-based questionnaire by elderly patients, within a controlled in-hospital setting is required, as a base for a telemedical approach.

Interventions

OTHERweb-based questionnaires

Patients will be asked to complete web-based questionnaires on a tablet computer

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Legally competent patients * Written informed consent * Age ≥ 65, male, female, diverse * Multimorbid patients (≥ 2 comorbidities (according to the Charlson Comorbidity Index) * Major elective surgery (such as total abdominal hysterectomy, endoscopic resection of prostate, lumbar discectomy, thyroidectomy, total joint replacement, lung operations, colon resection, radical neck dissection etc.)

Exclusion criteria

* Blind or deaf patients * Patient/ Proxy not able to use electronic devices e.g. computer, tablet or smart phone * Non-fluency in local language * Alcohol and/ or drugs abuse * Ambulatory surgery * Repeated surgery, with previous participation * Patients with severe neurological or psychiatric disorder * Refusal of study participation by the patient

Design outcomes

Primary

MeasureTime frameDescription
Completion rate1 dayThe completion rate of the total number of questions of the web-based questionnaires

Secondary

MeasureTime frameDescription
Assessment of the kind of patient's requests for help to the accompanying next of kin1 dayThe study team member, who is present during the study treatment, will assess the kind of the patient's requests for help to the accompanying next of kin, divided into: technical request or request regarding the content of the web-based questions
Assessment of the kind of patient's requests for help to the study team member1 dayThe study team member, who is present during the study treatment, will assess the kind of the patient's requests for help to himself, divided into: technical request or request regarding the content of the web-based questions
Frequency of patient's requests for help to the study team member1 dayThe study team member, who is present during the study treatment, will assess the frequency of the patient's requests for help to him
Frequency of patient's requests for help to the accompanying next of kin1 dayThe study team member, who is present during the study treatment, will assess the frequency of the patient's requests for help to the accompanying next of kin
Ranking of unanswered questions1 dayWe will analyse which questions where not answered by the most patients.
Patient satisfaction1 dayAnalysis of patient satisfaction about the web-based questionnaires. A paper-based satisfaction questionnaire is provided to the patient after the completion of the web-based survey. The satisfaction questionnaire will consist of a 5-point Likert scale. It will consist of the items: Strongly disagree; Disagree; Neither agree nor disagree; Agree; Strongly agree
Frequency of technical problems1 dayThe frequency of technical problems (i.e. internet connection, black screen etc.) will be assessed by the present study team member
Elapsed time for questionnaire completion1 dayThe survey software will automatically count the elapsed time for completion of the questionnaires. The time will start in the moment, when the patient accesses the website and it will end when he presses the finish button

Countries

Germany

Contacts

Primary ContactAna Kowark, MD
akowark@ukaachen.de+49241800

Outcome results

None listed

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