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OpenTrials
Completed

NCT Number: NCT04578587

Reliability of Hand Held Dynamometer for Assessing Isometric Lumbar Muscle Strength in Asymptomatic Healthy Population

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

Completed

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Key information

Conditions

Age range

21 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Lahore

Lahore, Punjab Province, 52132, Pakistan

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

MicroFET 2

Device

Lumbar Flexor and Extensor Strength Measurement

Primary outcomes

  1. Hand held dynamometer

    Time frame: 2 Weeks

    Muscle Strength

Sponsors and collaborators

Lead sponsor

Fahad Tanveer

Other

Registry information

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Oct 8, 2020
Registry last updated
Mar 25, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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