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Combination of Two Osteopathic Techniques for the Hamstring's Stretching Capacity in Basketball Female Players

N

Natália Maria Oliveira Campelo

Status

Not yet enrolling

Conditions

Healthy

Treatments

Other: Simulated technique
Other: 4th ventricle technique and muscular energy technique
Other: Muscle energy technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06357611
OST1_015

Details and patient eligibility

About

It is known that there are studies that prove the effectiveness of muscle energy techniques and the fourth ventricle technique separately, however, information is scarce regarding the combination of the two and their effectiveness in the population. The aim of this randomized controlled study is to compare the immediate effects of the techniques compared to the muscle energy technique alone in female basketball players.

Full description

The muscular energy technique (MET) is a manual therapy technique that uses isometric contractions with the aim of increasing the extensibility of the muscle group, as well as promoting lymphatic and venous circulation. The fourth ventricle technique (CV-four) plays an amplifying role in the movement of tissues and fluids, restoring the flexibility of the autonomous response. For the MET, the researcher adopted a position homolateral to the dominant limb, contacting the lower limb with the caudal hand in the region of the malleoli. He then helped the participant to perform the movement, which consisted of flexion of the hip and extension of the knee passively until the motor barrier was reached, after which she was instructed to perform an isometric contraction of the hamstring. A total of three contractions of seven seconds with an interval of two to three seconds were requested, using approximately twenty per cent of their maximum force, and gaining a new motor barrier between each series, for a total of three series. For the CV-four technique, the researcher adopted a seated position and laterally contacted the scaly portion of the occiput, bringing it closer to the posterior convexity of the occiput, bringing the skull into extension, changing the compression movement with decompression, until three minutes had elapsed. At all stages of the session, the participant was positioned in the supine position, with the upper limbs alongside the body and the neck in a neutral position. All the participants in the study underwent an initial and final assessment protocol to determine their range of motion (ROM).

Enrollment

34 estimated patients

Sex

Female

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over 18 years old
  • Female
  • Playing federated basketball
  • Signature of informed consent documents

Exclusion criteria

  • Surgical intervention/trauma in the areas of activity (cervical-cranial and lower limb)
  • Exposure to medicinal therapy
  • Participants with hypertension
  • Participants at risk of cerebral hemorrhage (e.g. aneurysm)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 3 patient groups, including a placebo group

Control Group
Placebo Comparator group
Description:
After completing an individual questionnaire and giving informed consent, a placebo technique was performed, consisting only of contact in the area of the participant's shoulders.
Treatment:
Other: Simulated technique
Experimental group MET
Experimental group
Description:
After completing an individual questionnaire and giving informed consent, the muscle energy technique was performed on the dominant hamstring muscle.
Treatment:
Other: Muscle energy technique
Experimental group CV-4 and MET
Experimental group
Description:
After completing an individual questionnaire and giving informed consent, the 4th ventricle technique (CV-4) was performed, followed by the muscle energy technique on the dominant hamstring muscle.
Treatment:
Other: 4th ventricle technique and muscular energy technique

Trial contacts and locations

1

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Central trial contact

Natália MO Campelo, PhD

Data sourced from clinicaltrials.gov

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