Actively Recruiting

Phase Not Applicable
Age: 21Years - 65Years
All Genders
ID03171012

Proprioceptive Neuromuscular Facilitation Effects With Cardiorespiratory Training in Stroke Patients on Motor, Respiratory Functions, and Quality of Life: Randomized Controlled Trial

Led by Universidade Federal do Rio Grande do Norte · Updated on 2023-05-11

40

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the effects of combining Proprioceptive Neuromuscular Facilitation (PNF) with cardiorespiratory training (CRT) on individuals who have hemiparesis following a stroke. This condition impacts limb function as well as the trunk and abdomen, reducing physical activity. The study aims to evaluate how PNF and CRT together might improve quality of life, gait, respiratory and motor functions, and other health measures in people with stroke-related hemiparesis. Forty participants post-stroke will be randomly assigned to one of four groups: lower limbs CRT with PNF, lower limbs CRT with respiration exercises, upper limbs CRT with PNF, or upper limbs CRT with respiration exercises. Each group will undergo 20 sessions of therapy lasting one hour each, including stretching, rest, and 40 minutes of aerobic treatment using a cycle ergometer for either the upper or lower limbs. PNF patterns and breathing exercises are performed in various positions to enhance trunk function. Participants will be assessed before the treatment, immediately after 20 sessions (about two months), and one month after completing therapy. Assessments include quality of life scales, gait analysis, oxygen consumption, respiratory muscle strength, diaphragm thickness, and rib cage volume measurements. Monitoring of heart rate, blood pressure, oxygen saturation, and perceived exertion will support safety and adherence throughout the program.

CONDITIONS

Brief Title

Addition of Proprioceptive Neuromuscular Facilitation to Cardio Respiratory Training Post Stroke

Who Can Participate

Age: 21Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of ischemic or hemorrhagic stroke with hemiparesis lasting more than six months
  • Mental competence confirmed by Mini-Exam of the Mental State (MMSE)
  • Ability to walk 10 meters independently, with or without assistive devices
  • Absence of other neurological or orthopedic deficits unrelated to stroke
  • No history of pulmonary disease and not a current or former smoker
  • Age between 21 and 65 years
Not Eligible

You will not qualify if you...

  • No additional exclusion criteria provided

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Approximately 7 weeks

Participants receive 20 sessions of cardiorespiratory training combined with either proprioceptive neuromuscular facilitation or respiration techniques. Each session lasts one hour and includes stretching, rest, and aerobic treatment performed three times a week over approximately 7 weeks.

20 therapy sessions, three times a week

Follow-up

Duration - 1 month

Participants are assessed one month after completing the treatment to evaluate the effects on motor and respiratory functions and quality of life.

1 follow-up visit

Trial Site Locations

Total: 1 location

1

Universidade Federal de Pernambuco

Recife, Pernambuco, Brazil, 50740 - 560

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Research Team

R

RENATA SOUZA, MASTER

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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Published Research Related To This Trial

Addition of proprioceptive neuromuscular facilitation to cardiorespiratory training in patients poststroke: study protocol for a randomized controlled trial.

Renata Janaína Pereira de Souza, Daniella Cunha Brandão, José Vicente Martins...

https://pubmed.ncbi.nlm.nih.gov/32059691