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Effects of Preoperative Relaxation and Intensified Surgery Education in Patients Undergoing Herniotomy (MBM_Hernio)

U

Universität Duisburg-Essen

Status

Unknown

Conditions

Postoperative Pain
Hernia, Inguinal
Anxiety

Treatments

Behavioral: surgery education
Behavioral: relaxation program

Study type

Interventional

Funder types

Other

Identifiers

NCT02476370
14-6060-BO MBM_Hernio

Details and patient eligibility

About

This study aims to test the effects of a Preoperative Relaxation intervention and an Intensified Surgery Patient Education on pre- and postoperative wellbeing and health in Patients Undergoing Herniotomy.

Full description

see above

Enrollment

108 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • referral for herniotomy
  • preoperative anxiety at least 4/10 points on a numeric rating scale
  • physical and mental capability to participant
  • written informed consent

Exclusion criteria

  • Emergency surgery
  • malignoma
  • recurrence of inaugural hernia
  • severe comorbidity
  • severy psychological disorders
  • immunosuppression
  • coagulation disorders

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

108 participants in 4 patient groups

Usual care
No Intervention group
Description:
Does not receive a specific study intervention
preoperative relaxation program
Experimental group
Description:
preoperative relaxation program
Treatment:
Behavioral: relaxation program
preoperative surgery education
Experimental group
Description:
single education unit to understand the complete surgical procedures
Treatment:
Behavioral: surgery education
preoperative relaxation program+preoperative surgery education
Experimental group
Description:
preoperative relaxation program AND single education unit
Treatment:
Behavioral: surgery education
Behavioral: relaxation program

Trial contacts and locations

1

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Central trial contact

Gustav Dobos, Prof, MD

Data sourced from clinicaltrials.gov

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