The impact of video-assisted preoperative patient information on patient-reported outcomes after pancreatic resection (INFORM Trial)

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

DRKS

Registry ID

DRKS00035173

Enrollment

Registered

2024-10-14

Start date

2024-10-14

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Pancreatic diseases

Interventions

Group 1: Video-based patient information in addition to the standard pre-operative preparations Group 2: no videos

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are scheduled for elective pancreatic resection (laparoscopic, robotic and open approach) for any indication; good knowledge of German; written informed consent

Exclusion criteria

Exclusion criteria: Inability to comply with visits and follow-ups; inability to understand the videos, participation in another study that could affect the study outcome

Design outcomes

Primary

Measure	Time frame
Feasibility	—

Secondary

Measure	Time frame
The secondary objectives are to evaluate quality of life (QLQ) in terms of (i) satisfaction with information on disease and treatment as assessed by the validated questionnaire by the European Organisation For Research and Treatment of Cancer (EORTC) QLQ – INFO25, and (ii) disease symtoms as assessed by EORTC QLQ C30 and PAN26. In addition, morbidity and mortality will be assessed.	—

Countries

Austria

Contacts

Public ContactUlla Klaiber

Medizinische Universität Wien

ulla.klaiber@meduniwien.ac.at+4314040056470

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026