NCT04578587

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Jul 2020

Shorter than P25 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 15, 2020

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2020

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

October 2, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 8, 2020

Completed
Last Updated

March 25, 2021

Status Verified

March 1, 2021

Enrollment Period

1 month

First QC Date

October 2, 2020

Last Update Submit

March 22, 2021

Conditions

Healthy

Keywords

ReliabilityLumbar regionMuscle strength dynamometer

Outcome Measures

Primary Outcomes (1)

  • Hand held dynamometer

    Muscle Strength

    2 Weeks

Study Arms (2)

Rater 1

ACTIVE COMPARATOR

Rater 1

Device: MicroFET 2

Rater 2

ACTIVE COMPARATOR

Rater 2

Device: MicroFET 2

Interventions

MicroFET 2DEVICE

Lumbar Flexor and Extensor Strength Measurement

Rater 1Rater 2

Eligibility Criteria

Age21 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • age between twenty one to twenty five years

You may not qualify if:

  • subjects with the history of acute, subacute or chronic low back pain, history of trauma, neurological disorders, spinal surgery, lumbar spine pathology were excluded.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Lahore

Lahore, Punjab Province, 52132, Pakistan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

October 2, 2020

First Posted

October 8, 2020

Study Start

July 15, 2020

Primary Completion

August 15, 2020

Study Completion

August 15, 2020

Last Updated

March 25, 2021

Record last verified: 2021-03

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)