"Reliability of Motricity Index Strength Assessments for Upper Extremity in Post Stroke Hemiparesis- a Correlation Study''

Stroke Clinical Trial

Official title:

"Reliability of Motricity Index Strength Assessments for Upper Extremity in Post Stroke Hemiparesis- a Correlation Study''

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02353520
• Other study ID #: RELIBILITY OF MOTRICITY INDEX
• Status: Completed
• Phase: N/A
• First received: January 28, 2015
• Last updated: January 30, 2015
• Start date: June 2013
• Est. completion date: July 2014

Study information

• Verified date: January 2015
• Source: Maharishi Markendeswar University
• Contact: n/a
• Is FDA regulated: No
• Health authority: India: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

Initially, a written consent was obtained from each participant. Then they became familiar with the procedure. For intrarater reliability, the first rater assessed the strength of pinch grip, elbow flexion and shoulder abduction in three different sessions at short intervals on same day in same environmental conditions. All the assessments were performed on the same day in three sessions. Assessment duration of all the sessions was 5 minutes.

For inter-rater reliability, Before the beginning of Procedure both the raters were familiarized with the motricity index. The motricity index was administered by two different raters on the same subjects within 2 days who were blind to each others results and heir results were recorded separately.

Description:

Initially, a written consent was obtained from each participant. Then they became familiar with the procedure. For intrarater reliability, the first rater assessed the strength of pinch grip, elbow flexion and shoulder abduction in three different sessions at short intervals on same day in same environmental conditions. All the assessments were performed on the same day in three sessions. Assessment duration of all the sessions was 5 minutes.

For inter-rater reliability, Before the beginning of Procedure both the raters were familiarized with the motricity index. The motricity index was administered by two different raters on the same subjects within 2 days who were blind to each others results and heir results were recorded separately.

PATIENT POSITION The patient was sitting on a chair or on the edge of the bed, but can be tested lying supine if necessary. In the arm the three movements tested were pinch grip, elbow flexion and shoulder abduction.

Pinch grip Assessed by asking the patient to grip a 2.5 cm cube between the thumb and fore finger. The object was on a flat surface (for example, a book).

The tester scored contraction of any forearm or small hand muscles as follows:

0 No movement. 11 Beginnings of prehension (any movement of finger or thumb). 19 Able to grip the cube, but not hold it against gravity (examiner may need to lift the wrist) 22 Able to grip and hold the cube against gravity, but not against a weak pull.

26 Able to grip and hold the cube against a weak pull, but weaker than the other side.

33 Normal pinch grips. Elbow flexion The elbow was tested with the elbow flexed to 90°, forearm horizontal and upper arm vertical. The patient was asked to bend the elbow so that the hand touches the shoulder. The examiner resisted with a hand on the wrist, and monitored the biceps. If there was no movement, the examiner holded the elbow out so that the arm was horizontal, and gave a score of 14 if movement was then seen.

Shoulder abduction The elbow was fully flexed and against the chest and the patient was asked to abduct the arm. The examiner monitored contraction of the deltoid movement of shoulder girdle does not count-there must be movement of humerus in relation to scapula). A score of 19 was given when the shoulder was abducted to more than 90◦ beyond the horizontal against gravity but not against resistance.

According to the quality of muscle contraction the score was recorded. Rater was also aware of any trick motion such as leaning the back during the movement by placing one hand on their back. Finally, all three scores were summed and the Motricity Index for upper extremity was calculated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: July 2014
• Est. primary completion date: April 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 37 Years to 76 Years

Eligibility

Inclusion Criteria:

1. Post stroke hemiparetic patients were included in the study.

2. Age 37 to 76 years.

3. Mini mental status examination score = 23.

4. Individuals having Brunnstrom stage 4 and 5 in upper extremity.

5. Individuals should not be taking any physiotherapy treatment for stroke

Exclusion Criteria:

1. Patients at the acute or chronic commonly seen at clinics.

2. Patient having any musculo-skeletal disorder in upper limb.

3. Patient having any trauma on their upper extremity.

4. Patient having any neurological disorder other than stroke.

5. Any hypersensitivity or hyposensitivity disorder

Study Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Stroke

Intervention

Other:
• motricity index strength assessment

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Maharishi Markendeswar University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Motricity index strength assessment	Initially, a written consent was obtained from each participant. Then they became familiar with the procedure. For intrarater reliability, the first rater assessed the strength of pinch grip, elbow flexion and shoulder abduction in three different sessions at short intervals on same day in same environmental conditions. All the assessments were performed on the same day in three sessions. Assessment duration of all the sessions was 5 minutes.; For inter-rater reliability, Before the beginning of Procedure both the raters were familiarized with the motricity index. The motricity index was administered by two different raters on the same subjects within 2 days who were blind to each others results and heir results were recorded separately.	1 month	Yes