Effects of the Proprioceptive Neuromuscular Facilitation for Promoting Muscular Irradiation
1 other identifier
interventional
24
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2016
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2016
CompletedFirst Submitted
Initial submission to the registry
June 22, 2016
CompletedFirst Posted
Study publicly available on registry
July 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2016
CompletedJune 14, 2019
June 1, 2019
3 months
June 22, 2016
June 12, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Muscular activity by means of Electromyography
Muscular activity will be assessed in the left lower limb
Change from pre to post intervention (at least 40 min)
Study Arms (5)
Upper limb pattern
EXPERIMENTALUpper Limb pattern with flexion - abduction - external rotation
Lower limb pattern 1
EXPERIMENTALLower Limb pattern with flexion - adduction - external rotation with knee flexion;
Lower limb pattern 2
EXPERIMENTALLower Limb pattern with flexion - abduction - internal rotation with knee flexion;
Lifting to the right
EXPERIMENTALSit to Stand
ACTIVE COMPARATORSit to Stand task
Interventions
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".
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".
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".
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".
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.
Eligibility Criteria
You may qualify if:
- right-handed
- sedentary
- healthy
- body mass index between 18.5 - 24.9 kg/m2
You may not qualify if:
- having any injuries that prevented the implementation of the proposed activities
- being pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Federal University of Health Sciences of Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
June 22, 2016
First Posted
July 1, 2016
Study Start
June 1, 2016
Primary Completion
September 1, 2016
Study Completion
September 1, 2016
Last Updated
June 14, 2019
Record last verified: 2019-06