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SUBSTITUTION OF USUAL PERIOPERATIVE CARE BY E-HEALTH & ICT; a cost-effectiveness analysis

SUBSTITUTION OF USUAL PERIOPERATIVE CARE BY E-HEALTH & ICT; a cost-effectiveness analysis - I recover 3

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON53164
Enrollment
685
Registered
2016-05-17
Start date
2015-08-08
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

herstel na operaties Perioperative care

Interventions

Patients in the intervention group will receive a special perioperative care program. This care program consists of: 1. E-health intervention (webportal and accelerometer) 1.1 Personalized convalesc
Convalescence
Cost-effectiveness
Perioperative care

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: All patients aged from 18 to 70 years old who are on the waiting list for a laparoscopic cholecystectomy, an open or laparoscopic colectomy, an open or laparoscopic appendectomy, open or laparoscopic inguinal hernia surgery, an abdominal or laparoscopic hysterectomy or laparoscopic adnexal surgery. Due to differences in surgical procedures we identify two subgroups in the study population: Subgroup 1: Patients who are on the waiting list for a laparoscopic cholecystectomy, an open or laparoscopic appendectomy, open or laparoscopic inguinal hernia surgery or laparoscopic adnexal surgery. Subgroup 2: Patients who are on the waiting list for an open or laparoscopic colectomy, or an abdominal or laparoscopic hysterectomy.

Exclusion criteria

Exclusion criteria: • Surgery without a curative intention or with additional radio- or chemotherapy • Colectomy because of crohn*s disease or ulcerative colitis • Deep infiltrating endometriosis • Perforated appendicitis • Adnexal surgery because of pelvic inflammatory disease/ tubal ovarian abces • Combination of surgery with other surgical procedures • Concomitant health problems affecting daily activities • Severe comorbidity which might complicate the postoperative course • Patients who are unable to understand the information belonging the research • Insufficient understanding or ability to fill in (Dutch) questionnaires

Design outcomes

Primary

MeasureTime frame
1.Quality-of-life (Rand 36 or EQ-5D) 2.Return-to-normal activities including work (RNA/RTW) according to WHO definition of social participation (ICF, 40)

Secondary

MeasureTime frame
- Return to physical activities - Return to work - Length of recovery - Empowerment - Pain intensity - Patients satisfaction - Protocol adherence - Quality improvement

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)