ClinicalTrials.gg
Not yet recruitingNCT06872554Updated Mar 12, 2025

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

An interventional study of Supervised exercise training and Non supervised exercise training in Abdominal Wall Hernia, Prevention and Exercise, sponsored by University of Seville. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-12.

Sponsored by University of Seville · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

Background:

Abdominal wall hernias are one of the most prevalent pathologies in contemporary clinical practice, affecting a significant percentage of the global population. These hernias, characterized by the protrusion of organs or tissues through a weakened area in the abdominal musculature, may present symptoms such as pain, tightness, and gastrointestinal complications, impacting both general health and patients' quality of life. The management of these conditions often involves surgical intervention, with variable outcomes in terms of functional recovery and postoperative pain. However, there are still opportunities to improve preoperative and postoperative treatment strategies through comprehensive approaches that include adapted physical training programs.

In recent years, the field of physical rehabilitation has advanced significantly due to the development of multicomponent training programs. These programs, combining strength, mobility, and stretching exercises, have proven effective in improving quality of life and reducing pain in various chronic pathologies. For instance, in patients with osteoarthritis, multicomponent training has been shown not only to mitigate pain but also to improve functional capacity and reduce progressive joint deterioration. In sarcopenia, a common problem in older adults, resistance training has demonstrated significant benefits in maintaining muscle mass and strength, contributing to a better quality of life.

Moreover, participation in prehabilitation programs has been particularly beneficial in the context of surgical procedures. Recent studies have documented that patients undergoing anterior cruciate ligament or meniscal interventions who participated in multicomponent prehabilitation programs experienced less strength and muscle mass loss, as well as a reduced perception of postoperative pain. A recent meta-analysis also shows that prehabilitation programs including strength training and aerobic exercises contributed to improved functional outcomes and shorter hospital stays in patients undergoing major abdominal surgery. This proactive approach, which prepares the body for surgical stress, has proven to be an effective strategy for improving postoperative outcomes and accelerating recovery.

However, despite evidence supporting the use of multicomponent training programs in other clinical and surgical conditions, their application in patients with abdominal wall hernias has been scarcely explored. The current literature lacks studies that comprehensively address the impact of prehabilitation in this patient group, both in the preoperative phase and postoperative recovery. Given that hernia repair surgery is one of the most common surgical interventions, with significant implications for functional capacity and overall well-being, implementing prehabilitation strategies based on multicomponent training could represent an important innovation in managing these conditions.

In conclusion, this study proposes that a multicomponent prehabilitation program could not only improve functional capacity and reduce preoperative pain in patients with abdominal wall hernias but also optimize postoperative outcomes and overall recovery. This approach is based on accumulated evidence in other clinical and surgical fields, reinforcing the need to explore its applicability and effectiveness in this specific context.

Study Objectives:

Evaluate the effects of a multicomponent training program on strength levels, quality of life, and pain in patients with abdominal wall hernias.

Assess the effects of the multicomponent training program on the aforementioned variables post-abdominal wall surgery.

Determine how the intervention affects hospital stay duration and postoperative complications.

Analyze differences between supervised and unsupervised training programs.

Compare postoperative functional recovery between the intervention and control groups.

Methodology:

An experimental, prospective, and longitudinal study will be conducted, implementing a multicomponent training program over 12 weeks. Patients will be recruited from the Abdominal Wall Surgery Unit of Virgen del Rocío Hospital.

Inclusión Criteria:

Patients ≥ 18 years; Ventral hernia ≥ 4cm (W2-3 per EHS classification); Signed informed consent.

Exclusión Criteria:

Patients \<18 years; Ventral hernia \<4cm (W1 per EHS classification); Severe physical/cognitive impairment affecting mobility and daily activities.

Study Phases:

  1. Patient Recruitment: Eligible patients will be randomized into three groups: supervised intervention, online intervention, and control.
  2. Data Collection: Muscle strength, pain, quality of life, perceived exertion, and body composition will be evaluated pre-intervention, post-intervention, and three months post-surgery.
  3. Statistical Analysis: Descriptive and multivariate statistical models will be applied to determine associations between intervention and study variables.
02

Conditions studied

  • Abdominal Wall Hernia
  • Prevention
  • Exercise
  • Physical Activity

Keywords

  • hernia
  • abdominal wall
  • exercise intervention
  • quality of life
  • pain
  • incisional hernial
03

In context

Hernia, Abdominal

82 studies on the registry are indexed under Hernia, Abdominal; 19 are open to participants now.

This study's planned enrollment of 75 is below the median of 90 across 48 interventional studies indexed under Hernia, Abdominal.

Browse Hernia, Abdominal studies →

Lead sponsor

University of Seville is the lead sponsor of 130 studies on the registry; 39 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients ≥ 18 years
  • Ventral hernia ≥ 4cm (W2-3 per EHS classification)
  • Signed

Exclusion criteria

Exclusion Criteria:

  • Patients \<18 years
  • Ventral hernia \<4cm (W1 per EHS classification)
  • Severe physical/cognitive impairment affecting mobility and daily activities
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Supervised Exercise Intervention

    Group that will follow the 12-week training program supervised by a professional in physical activity and sports sciences.

    Other: Supervised exercise training

  • Active comparator
    Non Supervised Exercise Intervention

    Group that will follow the 12-week training program from home, without the supervision of a professional in physical activity and sports sciences.

    Other: Non supervised exercise training

  • No intervention
    Control Group

    Participants randomly assigned to the control group will receive advice on the importance of an active lifestyle for their quality of life.

Interventions

  • OtherSupervised exercise training

    The intervention will consist of a 12-week multicomponent training program. This program will include exercises focused on strength training, mobility, stretching, and breathing. Throughout the 12 weeks, there will be a progressive increase in training volume-understood as the number of sets and repetitions performed-and in intensity, defined as the difficulty involved in performing the exercises. After each training session, data will be collected on the perceived effort and the pain in the area affected by the abdominal hernia.

  • OtherNon supervised exercise training

    The intervention will consist of a 12-week multicomponent training program. This program will include exercises focused on strength training, mobility, stretching, and breathing. Throughout the 12 weeks, there will be a progressive increase in training volume-understood as the number of sets and repetitions performed-and in intensity, defined as the difficulty involved in performing the exercises. After each training session, data will be collected on the perceived effort and the pain in the area affected by the abdominal hernia. This program will be realized for the participants at home, with the use of a specified training App, without the supervision of a sport science professional.

06

What researchers measure

Primary outcomes

  1. Abdominal Muscles Wall Strength

    To assess the strength of the abdominal wall muscles, the isometric trunk flexion test in a seated position will be used, both in the sagittal and transverse planes, utilizing a strain gauge (Chronojump, Barcelona, Spain). The variables collected will be the maximum isometric strength and the rate of force development.

    Time frame: Pre (0 week), Post (12 week), Post Surgery (3 month)

  2. Health Releated Quality of Life

    Quality of life will be assessed using a specific questionnaire for abdominal wall hernias (HerQLes) and a general questionnaire (SF 12)

    Time frame: Pre (0 week), Post (12 week), Post Surgery (1 month), Post Surgery (3 month)

  3. Pain

    Pain will be assessed using a visual analog scale (VAS), where 0 represents no pain and 10 represents maximum pain.

    Time frame: Pre (0 week), Post (12 week), Post Surgery (1 month), Post Surgery (3 month)

Secondary outcomes

  1. Physical Activity Level

    The level of physical activity will be assessed using the IPAQ Short Version questionnaire, which assess the physical activity on the las 7 days.

    Time frame: Pre (0 week)

  2. Sedentary Behaviour

    The level of sedentary behavior will be assessed using the Sedentary Behavior Questionnaire (SBQ), which evaluates the time a person spends sitting on weekdays and weekends.

    Time frame: Pre (0 week)

  3. Physical Performance

    To assess physical abilities, three tests from the Senior Fitness Test will be used: handgrip strength, sit-to-stand in 30 seconds, and walking speed over 4 meters.

    Time frame: Pre (0 week), Post (12 week), Post Surgery (3 month)

  4. Body Composition

    Muscle mass, fat mass, weight, and body mass index (BMI) will be evaluated using a digital bioimpedance scale (TANITA BC 545N).

    Time frame: Pre (0 week), Post (12 week), Post Surgery (3 month)

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided — Once processing, quality control, analysis and publication are complete, the data will be made accessible in open access repositories. These data will be anonymized (remove potentially identifying information).

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06872554
Collaborators
University Hospital Virgen del Rocio, Sevilla
Responsible party
Borja Sañudo (Head of the Department of Physical Education and Sport, University of Seville) — Principal investigator
First posted
Mar 12, 2025
Start date
Apr 15, 2025 (estimated)
Primary completion
Sep 15, 2025 (estimated)
Completion
Dec 15, 2025 (estimated)
Last update
Mar 12, 2025

Study contacts

Jose Luis Gil Delgado, Phd
Contact
luisdlgd3@gmail.com
+34654143004
Borja Sañudo Corrales, Phd
study director · University of Seville

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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