NCT04541784View on ClinicalTrials.gov

Effectiveness of an App Intervention to Reduce Postsurgical Symptom Distress in Patients With Vulvar Neoplasia

NACompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

May 1, 2019

Primary Completion Date

August 31, 2021

Study Completion Date

August 31, 2021

Conditions
Vulvar Neoplasm
Interventions
OTHER

WOMAN-PRO III

"Standardized care and three counselling sessions with a gynaecology-oncology nurse and the use of the mobile app WOMAN-PRO III."

OTHER

Three counselling sessions with gynaecology-oncology nurses

Standardized care, three counselling sessions with a gynaecology-oncology nurse.

Trial Locations (4)

3000

University Hospital of Bern, Bern

6000

Cantonal Hospital of Lucerne, Lucerne

6900

Regional Hospital of Lugano, Lugano

9000

Cantonal Hospital of St. Gallen, Sankt Gallen

All Listed Sponsors
collaborator

Cantonal Hospital of St. Gallen

OTHER

collaborator

Cantonal Hospital of Lucerne

UNKNOWN

collaborator

Regional Hospital of Lugano

UNKNOWN

collaborator

Insel Gruppe AG, University Hospital Bern

OTHER

lead

St.Gallen University of Applied Sciences

OTHER

NCT04541784 - Effectiveness of an App Intervention to Reduce Postsurgical Symptom Distress in Patients With Vulvar Neoplasia | Biotech Hunter | Biotech Hunter