Effects of Hipopressive Exercises in Nonspecific Low Back Pain

NCT ID: NCT03565926

Last Updated: 2025-07-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 64 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-01
• Study Completion Date: 2018-09-15

Brief Summary

Introduction Non-specific low back pain is very prevalent in our society. Different effective physiotherapy treatments have been performed in the reduction of pain and improvement of quality of life, however there are few studies that exist on the effectiveness of these treatments in protocol format based on manual therapy. On the other hand, there are no studies that implement a protocol of therapeutic exercises called abdominal hypopressives.

The aim of the study is to study the effect of a manual therapy protocol on non-specific low back pain and the implementation of hypopressive exercises in different areas such as disability, pain, flexibility and quality of life.

Material and methods

Participants The sample will consist of subjects with non-specific low back pain. Inclusion criteria

-Participants with nonspecific lumbar pain of at least 4 pain crises a month with recurrent low back pain.

Exclusion criteria

• Light acute.
• Lumbalgia after trauma.
• Presenting sciatica or musculoskeletal disorders or injuries within three months prior to the study.
• Contraindication of one of the two treatments.
• Participate in this period of no functional recovery program or physiotherapy treatment.

Study design A randomized clinical trial will be conducted. The sample will be divided into 2 groups: Group 1 will receive a manual therapy protocol that has previously shown its effectiveness in non-specific low back pain being 1 session a week, while group 2 will receive a protocol of hypopressive therapeutic exercises.

Evaluations

At the beginning of the study, a clinical interview will be carried out and, in addition, 3 evaluations will be carried out: at the beginning, at the end of the treatment and one follow-up per month. The investigators will use the following evaluation tools:

• Pain, through the Visual Analog Scale.
• Oswestry Low Back Pain Disability Scale.
• SF-36 quality of life scale.
• Visual Analog Scale.
• Algometry of spinous processes and lumbar muscles.
• Lumbar flexion with inclinometer and fingers test - floor.

Conditions

Low Back Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Manual Therapy

Manual Therapy Protocol

1. Articulation technique L4-S1

2. Lumbar neuromuscular technique

3. Fascial technique of crossed hands

4. Posteroanterior mobilizations of the lumbar vertebrae

Group Type: ACTIVE_COMPARATOR

Manual Therapy

Intervention Type: OTHER

1. Articulation technique L4-S1

2. Lumbar neuromuscular technique

3. Fascial technique of crossed hands

4. Posteroanterior mobilizations of the lumbar vertebrae

Hypopressive exercises

Protocol of 5 Hypopressive Exercises

Group Type: EXPERIMENTAL

Hypopressive exercises

Intervention Type: OTHER

Protocol 5 Hypopressive exercises

Interventions

Manual Therapy

1. Articulation technique L4-S1

2. Lumbar neuromuscular technique

3. Fascial technique of crossed hands

4. Posteroanterior mobilizations of the lumbar vertebrae

Intervention Type: OTHER

Hypopressive exercises

Protocol 5 Hypopressive exercises

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Man between 18 and 40 years old
• Recurrent episodes of low back pain at least 4 times a month
• At least 3 months of evolution
• Non-specific low back pain
• Not having undergone surgery

Exclusion Criteria

• Acute low back pain
• Lumbalgia operated surgically
• Low back pain after traumatism
• Episodes of sciatica
• Contraindication to any of the treatments
• Attend, during the study period, rehabilitation programs
• Serious injuries in the 3 months prior to the study
• Root pain

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Valencia

OTHER

Sponsor Role: lead

Responsible Party

GEMMA V ESPÍ LÓPEZ, PhD

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Gemma v. Espí López

Valencia, , Spain

Countries

Spain

Other Identifiers

ID0019

Identifier Type: -

Identifier Source: org_study_id