Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID03808584

Impact of Core Muscle Training on Incisional Hernia and Pain After Abdominal Surgery

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2026-05-05

588

Participants Needed

5

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the impact of core muscle training on the occurrence of incisional hernia, chronic postsurgical pain (CPSP), and sarcopenia after abdominal surgery. The study addresses the common practice of limiting core muscle activity post-surgery to prevent hernias, despite no evidence supporting this approach. The trial will explore whether physical restriction or specific core muscle exercises before and after surgery influence the incidence of incisional hernias and the development of CPSP and sarcopenia. Participants will be randomly assigned to one of two groups. The control group will receive standard physiotherapy, which includes early mobilization and exercises to prevent complications, while limiting core muscle activity and weight bearing based on pain. The intervention group will perform four specific core muscle exercises daily during hospitalization under physiotherapist supervision and continue at home for two months, alongside standard physiotherapy. Follow-up visits will occur at two, twelve, and twenty-four months post-surgery. During the study, participants will undergo clinical examinations and ultrasound scans to detect incisional hernias, assessments of chronic postsurgical pain and its treatment, and evaluations of muscle mass using CT scans. Researchers will also monitor exercise activity, hospital stay length, readmission and re-operation rates, and the incidence of sarcopenia. The study period includes regular follow-ups for up to two years to track these outcomes and evaluate the effects of postoperative rehabilitation.

CONDITIONS

Brief Title

Impact of Core Muscle Training on Incisional Hernia and Pain After Abdominal Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent
  • Age over 18 years
  • Capable of judgment
  • Undergoing elective or emergency abdominal surgery (laparoscopic or open, midline or transverse incision) at University Hospital of Bern, Kantonsspital Solothurn and Olten, BundeswehrZentralkrankenhaus Koblenz
  • Undergoing elective open abdominal surgery with midline or transverse incision at University Hospital of Lausanne
Not Eligible

You will not qualify if you...

  • Inability to follow study procedures due to language problems, psychological disorders, dementia, or similar
  • Investigator or related persons enrolled in the study
  • Neuromuscular diseases such as myasthenia gravis or wheelchair-bound status
  • Preexisting chronic pain disorder or chronic opioid therapy (WHO II and III) or use of pain-modulating drugs such as antidepressants or antiepileptics
  • End-stage disease
  • Presence of preexisting abdominal wall mesh, except inguinal mesh after hernia repair

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 2 months

Participants undergo abdominal surgery and receive either standard physiotherapy or specific core muscle exercises targeting abdominal muscles daily during hospitalization and continuing at home for two months after surgery.

Daily exercise under supervision during hospitalization and performed daily at home for two months

Follow-up

Duration - 24 months

Participants are followed up with clinical examinations, ultrasound to detect incisional hernias, assessments of chronic postsurgical pain, and evaluation of muscle mass on CT scans to monitor outcomes after surgery.

Visits at 2 months, 12 months, and 24 months after surgery

Trial Site Locations

Total: 5 locations

1

BundeswehrZentralkrankenhaus

Koblenz, Germany, 56070

Actively Recruiting

2

Kantonsspital Olten

Olten, Canton of Solothurn, Switzerland, 4600

Terminated

3

University Hospital of Bern, Inselspital

Bern, Switzerland, 3010

Actively Recruiting

4

CHUV, University Hospital of Lausanne

Lausanne, Switzerland, 1010

Actively Recruiting

5

Bürgerspital Solothurn

Solothurn, Switzerland, 4500

Withdrawn

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Research Team

G

Guido Beldi, MD

S

Stéphanie Perrodin, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

Preoperative inspiratory muscle training for postoperative pulmonary complications in adults undergoing cardiac and major abdominal surgery.

Morihiro Katsura, Akira Kuriyama, Taro Takeshima...

https://pubmed.ncbi.nlm.nih.gov/26436600

Surgery-Related Muscle Loss and Its Association with Postoperative Complications After Major Hepatectomy with Extrahepatic Bile Duct Resection.

Hidehiko Otsuji, Yukihiro Yokoyama, Tomoki Ebata...

https://pubmed.ncbi.nlm.nih.gov/27718001