- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02821598
Effects of the Proprioceptive Neuromuscular Facilitation for Promoting Muscular Irradiation
June 12, 2019 updated by: Aline de Souza Pagnussat, Federal University of Health Science of Porto Alegre
This study aims to evaluate the effects of Proprioceptive Neuromuscular Facilitation (PNF) patterns delivered to the upper limb, lower limb and trunk for promoting motor irradiation to the contralateral lower limb.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
24
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
-
-
Rio Grande Do Sul
-
Porto Alegre, Rio Grande Do Sul, Brazil
- Federal University of Health Sciences of Porto Alegre
-
-
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
18 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- right-handed
- sedentary
- healthy
- body mass index between 18.5 - 24.9 kg/m2
Exclusion Criteria:
- having any injuries that prevented the implementation of the proposed activities
- being pregnant
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: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Upper limb pattern
Upper Limb pattern with flexion - abduction - external rotation
|
The PNF pattern will be applied three times.
Participants will be in supine position under a stretcher, with arms folded and lower limbs in neutral position.
In order to induce irradiation for the contralateral lower limb, the left foot sole will be kept in contact with the wall.
For EMG recording, the participant will be positioned at the end of the PNF pattern and then the isometric contraction will be solicited.
The command used was: "do not let me move you".
|
|
Experimental: Lower limb pattern 1
Lower Limb pattern with flexion - adduction - external rotation with knee flexion;
|
The PNF pattern will be applied three times.
Participants will be in supine position under a stretcher, with arms folded and lower limbs in neutral position.
In order to induce irradiation for the contralateral lower limb, the left foot sole will be kept in contact with the wall.
For EMG recording, the participant will be positioned at the end of the PNF pattern and then the isometric contraction will be solicited.
The command used was: "do not let me move you".
|
|
Experimental: Lower limb pattern 2
Lower Limb pattern with flexion - abduction - internal rotation with knee flexion;
|
The PNF pattern will be applied three times.
Participants will be in supine position under a stretcher, with arms folded and lower limbs in neutral position.
In order to induce irradiation for the contralateral lower limb, the left foot sole will be kept in contact with the wall.
For EMG recording, the participant will be positioned at the end of the PNF pattern and then the isometric contraction will be solicited.
The command used was: "do not let me move you".
|
|
Experimental: Lifting to the right
|
The PNF pattern will be applied three times.
Participants will be in supine position under a stretcher, with arms folded and lower limbs in neutral position.
In order to induce irradiation for the contralateral lower limb, the left foot sole will be kept in contact with the wall.
For EMG recording, the participant will be positioned at the end of the PNF pattern and then the isometric contraction will be solicited.
The command used was: "do not let me move you".
|
|
Active Comparator: Sit to Stand
Sit to Stand task
|
Subjects will be sitting on a chair without armrests with ankles positioned at approximately 10 degrees of dorsiflexion.
Knees will be kept at approximately 100 degrees of flexion.
During the task, the participant will be instructed to stand from the sitting position while keeping their arms crossed over the chest.
The examiner will give the command "ready - set - go".
The task will be performed three times.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscular activity by means of Electromyography
Time Frame: Change from pre to post intervention (at least 40 min)
|
Muscular activity will be assessed in the left lower limb
|
Change from pre to post intervention (at least 40 min)
|
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
June 1, 2016
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
September 1, 2016
Study Registration Dates
First Submitted
June 22, 2016
First Submitted That Met QC Criteria
June 29, 2016
First Posted (Estimate)
July 1, 2016
Study Record Updates
Last Update Posted (Actual)
June 14, 2019
Last Update Submitted That Met QC Criteria
June 12, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 888.006
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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