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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04578587
Other study ID # IRB-UOL-FAHS/690/2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 15, 2020
Est. completion date August 15, 2020

Study information

Verified date March 2021
Source University of Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine intra-rater and inter-rater reliability of hand held dynamometer for assessing isometric lumbar


Description:

After being informed about the study and potential risks, all participants given informed consent underwent a 1-week screening period to determine eligibility for study entry. Two raters assessed isometric strength of lumbar flexor and extensor muscles, by a hand-held dynamometer. Strength was measured and recorded by each of the two raters and re-assessed after a week.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date August 15, 2020
Est. primary completion date August 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 25 Years
Eligibility Inclusion Criteria: - age between twenty one to twenty five years Exclusion Criteria: - subjects with the history of acute, subacute or chronic low back pain, history of trauma, neurological disorders, spinal surgery, lumbar spine pathology were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MicroFET 2
Lumbar Flexor and Extensor Strength Measurement

Locations

Country Name City State
Pakistan University of Lahore Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
Fahad Tanveer

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hand held dynamometer Muscle Strength 2 Weeks
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