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The effect of proprioceptive neuromuscular facilitation on cerebrovascular accident.

The effect of proprioceptive neuromuscular facilitation on muscle strength and activities of daily living of client with cerebrovascular accident .

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016043027676N1
Enrollment
60
Registered
2016-05-29
Start date
2016-05-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebrovascular Accident. Stroke, not specified as haemorrhage or infarction

Interventions

Intervention 1: Control group: First, while the experimental group, muscle strength and activities of daily living will be measured using the relevant protocol. Next any specific action on the contro
Rehabilitation
Control group: First, while the experimental group, muscle strength and activities of daily living will be measured using the relevant protocol. Next any specific action on the control, propriocepti
The intervention groups: First samples are available as a convenient choice then randomly allocated to two groups of test and control blocks would be allocated. Then the patients eligible for inclus

Sponsors

Yasouj University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Personal and informed consent to participate in the study; Residence in Yasouj; Over 4 months to 2 years after stroke; The definitive diagnosis of stroke by neurologist; Age over 60 years; One catching of stroke; No active phase of the disease; The absence of spinal cord injury; Lack of PNF techniques from six months ago; No other chronic diseases such as neurological disorders and orthopedic and rheumatology; Ability to communicate and answer questions Persian; The third and less muscle strength; Daily life activities less than 60 . Exclusion criteria: The unwillingness or inability of the Company to continue reading; Exacerbation or re CVA; The need for hospitalization; Physiotherapy at the same time; The occurrence of other diseases; Leave practice over two sessions; Death; Impairment of cognitive function; Mental alertness and presence of cognitive impairment during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Muscle strength. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Manual Muscle Testing grading scale.;Activities of Daily living. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Activities of Daily living Questionnaire.

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: The World Health Organization Quality of Life Questionnaire of 26 questions.;Muscle Strength. Timepoint: Before the intervention, Immediately after the intervention, One month after the intervention. Method of measurement: Digital Balance/Kg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParandvar Yaghoub

Martyr Dr.Beheshti hospital, Yasouj University of Medical Sciences and Health Services

yaghoub.parandvar@yums.ac.ir ; y.parandvar@gmail.com+98 74 3322 4721

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026