Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06811883

Optimising Hip Mobility, Hamstring Flexibility and Performance Using Lightback

Led by Universidad Católica de Ávila · Updated on 2025-02-06

20

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In athletics, in the sprint and hurdles disciplines, muscle injuries account for a significant proportion of injuries. The hamstrings are particularly vulnerable, accounting for between 12% and 26% of all injuries in these sports. A single-blind study was conducted on 20 hurdler patients with the intention of assessing hip mobility, hamstring flexibility and performance. To collect this data, the research team will conduct examinations and interviews with the athletes in two groups: an experimental group using LightBack and a placebo group.

CONDITIONS

Official Title

Optimising Hip Mobility, Hamstring Flexibility and Performance Using Lightback

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Sprinters and hurdlers aged 18 to 30 years
  • No history of recent (less than 6 months) hamstring or hip injury
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Cruciate or hamstring tears less than 6 months old
  • Hip and back surgery less than 3 months old
  • Chronic or acute back problems
  • Pregnancy
  • Osteoporosis
  • Tumours, bone cancer of the hip and pelvis
  • Direct trauma to the back of the thigh less than 6 months old
  • Orthopaedic or neurological pathologies affecting mobility or muscle activation
  • Participation in another specific training protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Universidad Pontificia de Salamanca

Salamanca, Spain, 27005

Actively Recruiting

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Research Team

J

JORGE Velázquez Saornil, PhD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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