Inter-rater reliability of the instrumented lean-and-release (iLEAN) test for manual assessment of reactive balance: A pilot study in simulated older adults

Abstract

Background and Purpose Quantitative assessment of reactive balance often requires large, costly equipment, limiting its use in clinical practice. This study investigated the inter-rater reliability of the instrumented lean-and-release (iLEAN) test, a manual reactive balance assessment designed to provide a practical alternative for physiotherapists.

Methods Sixteen healthy young women wore knee braces, weighted vests, and ankle weights to simulate reduced physical function typical of older adults. Participants completed the iLEAN test in standing, where reactive balance control was assessed in forward, left, right, and backward directions. During tests, an assessor applied the iLEAN device against the shoulder and released support once the participant reached a target lean load, which was progressively increased until balance could not be regained with a single step. Inter-rater reliability was analyzed using intraclass correlation coefficients (ICC, model 2,1) and Bland–Altman plots.

Results The ICCs (95% confidence intervals) for the iLEAN scores were 0.60 (0.17– 0.84) for forward, 0.75 (0.34–0.92) for left, 0.80 (0.45–0.94) for right, and 0.83 (0.58– 0.94) for backward. Bland–Altman analysis revealed no systematic bias between raters across all directions.

Discussion The iLEAN demonstrated acceptable inter-rater reliability in all directions, with the backward test showing the highest consistency. These findings suggest the iLEAN, particularly in the backward direction, may provide physiotherapists with a reliable and practical method to monitor changes in reactive balance control during exercise or rehabilitation, without reliance on specialized laboratory equipment.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was approved by the Office of Research Ethics at Kanagawa University of Human Services (Approval No. 18-23-34).

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors.

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