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Ultrasonography Biofeedback for Diaphragm Training in Athletes With Lumbo-pelvic Pain

U

Universidad de León

Status

Unknown

Conditions

Ultrasonography
Low Back Pain

Treatments

Other: Experimental
Other: Active comparator

Study type

Interventional

Funder types

Other

Identifiers

NCT04097392
UCM PR65/19

Details and patient eligibility

About

Objective: To determine the effectiveness of diaphragm biofeedback reeducation by ultrasonography in conjunction with high-intensity inspiratory muscle training versus isolated high-intensity inspiratory muscle training in athletes with lumbo-pelvic pain. Methods: A single blinded randomized clinical trial will be carried out. A total sample of 80 athletes with lumbo-pelvic pain will be recruited and randomized into 2 groups: one group will be treated by isolated high-intensity inspiratory muscle training during 8 weeks, and another group will be treated with diaphragm biofeedback reeducation by ultrasonography during 6 weeks in conjunction with high-intensity inspiratory muscle training during 8 weeks. Outcome measurements will be diaphragm muscle thickness evaluated by ultrasonography (main outcome measurement), pain intensity, pressure pain threshold, disability, quality of life and respiratory parameters by spirometry, which will be assessed before and after intervention.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Athletes with non-specific lumbopelvic pain during 6 weeks

Exclusion criteria

  • Neural disorders
  • Systemic disorders
  • Cognitive disorders

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Diaphragm biofeedback reeducation plus inspiratory training
Experimental group
Treatment:
Other: Experimental
Isolated high-intensity inspiratory muscle training
Active Comparator group
Treatment:
Other: Active comparator

Trial contacts and locations

1

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Central trial contact

César Calvo Lobo, PhD

Data sourced from clinicaltrials.gov

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