Improving the preoperative status of patients undergoing major surgery

Improving the preoperative status of patients undergoing major surgery - IMPRESS

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON53078

Enrollment

580

Registered

2018-07-19

Start date

2018-11-22

Completion date

Unknown

Last updated

2024-06-11

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

Conditions

major invasive surgery

Interventions

Use of an eHealth application for prehabilitation of surgical patients in the preoperative period. The intervention group is compared to control subjects receiving usual care.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age >= 18 years old Indication for postoperative hospital stay (minimum of two nights) One or more lifestyle risk factor Informed consent

Exclusion criteria

Exclusion criteria: Emergency surgery Unable to work with the eHealth application Dutch language inproficiency No access to a tablet or smartphone Planned for brain surgery Less than 7 days between inclusion and surgery Already participating in intensive pre-operative care pathway (including exercise program) Already participating in a conflicting study (to be determined per participating center)

Design outcomes

Primary

Measure	Time frame
(1) The main study endpoint is on feasibility. Feasibility of the use of BeterVoorbereid* application will be assessed by usability questions (Net promotor score and other usability questions; all patients in the intervention arm) and by semi-structured telephone interviews (random selection of 20 patients in the intervention arm). (2) The main study endpoint is effectiveness. The effectiveness will be evaluates using a physical functioning questionnaire on several timepoints, until 12 weeks after hospital discharge	—

Measure

Time frame

(1) The main study endpoint is on feasibility. Feasibility of the use of BeterVoorbereid* application will be assessed by usability questions (Net promotor score and other usability questions; all patients in the intervention arm) and by semi-structured telephone interviews (random selection of 20 patients in the intervention arm). (2) The main study endpoint is effectiveness. The effectiveness will be evaluates using a physical functioning questionnaire on several timepoints, until 12 weeks after hospital discharge

—

Secondary

Measure	Time frame
(1) we explore whether the use of this eHealth app leads to changes in preoperative lifestyle (i.e. exercise and/or smoking cessation and/or and/or nutrition) compared to control patients. Feasibility of the study procedures will be assessed using registration of patient recruitment and participation and monitoring of data collection. (2) 'global health', patient satisfaction, global perceived effect, lifestyle changes, length of hospital stay, postoperative complications	—

Measure

Time frame

(1) we explore whether the use of this eHealth app leads to changes in preoperative lifestyle (i.e. exercise and/or smoking cessation and/or and/or nutrition) compared to control patients. Feasibility of the study procedures will be assessed using registration of patient recruitment and participation and monitoring of data collection. (2) 'global health', patient satisfaction, global perceived effect, lifestyle changes, length of hospital stay, postoperative complications

—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)