Effects of a Multicomponent Training Program on Health Outcomes in Patients with Abdominal Wall Hernia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Seville

About this trial

Abdominal wall hernias are among the most prevalent pathologies today, characterized by specific symptoms such as pain, a sensation of tightness in the affected area, and potential gastrointestinal complications. These symptoms negatively impact patients' health and quality of life.

In other clinical conditions, such as osteoarthritis, sarcopenia, and fibromyalgia, participation in multicomponent training programs (which integrate strength, mobility, and stretching exercises) has been documented to significantly improve quality of life, reduce pain, and optimize patients' functional capacity. Likewise, scientific literature highlights that in the context of injuries requiring surgical intervention, such as anterior cruciate ligament or meniscus tears, patients who underwent prehabilitation programs based on multicomponent training experienced fewer losses in functional and structural aspects, such as strength and muscle mass. These programs also contributed to a reduction in postoperative pain perception.

Therefore, the primary objective of this study is to evaluate the effects of a multicomponent training program on health variables (pain, quality of life, perceived exertion, and recurrence) and functional capacity (trunk isometric strength, grip strength, and lower limb dynamic strength) in patients with abdominal wall hernias. As a secondary objective, the impact of this program on the aforementioned variables after abdominal wall repair surgery will be investigated.

Eligibility criteria

Qualifiers

Patients ≥ 18 years

Ventral hernia ≥ 4cm (W2-3 per EHS classification)

Signed informed consent

Disqualifiers

Patients <18 years

Ventral hernia <4cm (W1 per EHS classification)

Severe physical/cognitive impairment affecting mobility and daily activities

Trial design

Treatments tested in this trial

  • Supervised exercise training
  • Non supervised exercise training

Treatment groups

75 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

University of Seville

Lead sponsor

Hospitales Universitarios Virgen del Rocío

Collaborator