Manual Therapy and Proprioceptive Neuromuscular Facilitation in Field Hockey Players. (MTPNFHockeyP)

June 24, 2017 updated by: GEMMA V ESPÍ LÓPEZ, PhD, University of Valencia

Effectiveness of a Protocol Manual Therapy and Proprioceptive Neuromuscular Facilitation in Field Hockey Players.

Introduction: Field hockey is a contact sport. Semiflexion asymmetric position, along with other theories such as the weakness of the extensor muscles of the back or hamstring injury, can be causes or aggravating that suelan hockey players suffer back pain. Objectives: To observe the effectiveness of manual therapy techniques and post-isometric stretching (PNF) after three treatment sessions. In turn, know which of the two treatments have a greater benefit and longer. Methods: The population consists of grass hockey players and senior category aged between 16-30 years. They were randomly divided into two treatment groups. Group 1 corresponded to manual therapy techniques and group 2 to PNF stretching. The study duration for each subject was 5 sessions that included 3 treatment and 3 assessments. Each evaluation consisted of goniometry, balance test using the Sit and Reach, and Roland Morris questionnaire.

Study Overview

Study Type

Interventional

Enrollment (Actual)

47

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Valencia, Spain, 46010
        • Gemma Espí López

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 30 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • field hockey players (HH) (senior category).
  • between 16 and 30 years.
  • suffered injuries and microtraumatic not prevent them from sports.

Exclusion Criteria:

  • subjects with structural abnormalities of the spine.
  • plantar alterations.
  • other moderate or severe musculoskeletal previous injuries in the last 6 months and prevented them make sport normally.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Manual Therapy
The objective of treatment is to restore esta possible limitation of global mobility to major lower limb joints and remove any tensions from the musculature involved in a relevant way in this sport.
The patient remained lying on the gurney and the treatment was performed in the order set forth below and included: overall bilateral manipulation of L5-S1-Sacroiliac, subsequently decompression hip joint, the tibiofemoral decompression, stretching rotators hip flexion or hip and knee mobilization technique downing head and base of the fibula, tibiofibular-talus tali posteriorización decompression and with the help of a wedge to facilitate technical.
Active Comparator: Proprioceptive neuromuscular facilitation
It is a stretching technique with the aim of increasing the ROM. It includes passive static stretching and contract-relax.
Stretching were conducted in the hamstrings, psoas, adductors, pyramidal, quadriceps and right above.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dynamic balance
Time Frame: 6 weeks
Was assessed using the Star Excursion Balance Test (SEBT), Which bilateral in the above (A), posteromedial (PM) and posterolateral (PL) Were used reach directions.
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Range of Moviment
Time Frame: 6 weeks
Goniometry of both legs with universal goniometer external and internal rotation of the hip, hip flexion, knee flexion and ankle dorsiflexion.
6 weeks
Lumbar flexibility
Time Frame: 6 weeks
Was assessed using the Fingertip-to-Floor Test (FFT). Subjects were placed barefoot over a 25-cm high platform, with feet together and flat, and toes on the edge pointing forward. Then, they were asked to bend the trunk from the upright position as far as possible without discomfort, while maintaining knees and arms fully extended. Flexion was held for 3 seconds and the vertical distance between the tip of the middle finger and the platform was measured.
6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2016

Primary Completion (Actual)

September 1, 2016

Study Completion (Actual)

October 1, 2016

Study Registration Dates

First Submitted

August 8, 2016

First Submitted That Met QC Criteria

August 12, 2016

First Posted (Estimate)

August 17, 2016

Study Record Updates

Last Update Posted (Actual)

June 27, 2017

Last Update Submitted That Met QC Criteria

June 24, 2017

Last Verified

June 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • ID014

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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