Turkish Validation and Reliability of the John Hopkins In-Room Independence Scale

February 25, 2026 updated by: Selda Çiftci, Sisli Hamidiye Etfal Training and Research Hospital

Turkish Validity and Reliability Study of the John Hopkins In-Room Independence Scale: A Cross-Sectional Diagnostic Value Study

The aim was to conduct a Turkish validity and reliability study of the Johns Hopkins In-Room Independence Scale. The investigators believe this scale will address the lack of information regarding fall risk and dependency, particularly for patients scheduled for discharge and their caregivers.

Study Overview

Detailed Description

Independence and fall risk are critical for many illnesses and age groups. Patients receiving inpatient physical therapy in a Physical Medicine and Rehabilitation clinic often worry about returning home and performing daily activities after discharge. Therefore, this scale assessing in-room independence will allow clinicians to better warn and guide patients about potential risks.

Study Type

Observational

Enrollment (Actual)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey (Türkiye)
        • Sisli Hamidiye Etfal Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients aged 18 and over who are receiving inpatient treatment in the PM&R service with any diagnosis

Description

Inclusion Criteria:

  • Ages 18 and over
  • Volunteering to participate in the study

Exclusion Criteria:

  • Patients <18 years old

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients receiving treatment in a physical medicine and rehabilitation inpatient clinic
Patients aged 18 and over who are receiving inpatient treatment at the PM&R inpatient clinic with any diagnosis
The Turkish validity and reliability study of The Johns Hopkins Hospital In-Room Independence Scale(JH-IRIS) will be conducted.The researchers who developed the scale were contacted and a two-stage translation was conducted based on their suggestions.The final Turkish version of the scale was agreed upon after an online meeting with the developing research group.Because the other scales used in the original study lacked Turkish validity, the decision was made to use the Turkish-validated Morse and Henrich-2 Fall Scales and the Barthel Index, with the research team's permission.The study planned to include patients hospitalized for rehabilitation over a four-month period, regardless of their indication.This will allow comparison with previously validated Turkish fall risk and independence scales.One week later, patients will complete the JH-IRIS again and undergo a test-retest.The scale will be evaluated by two different researchers to determine inter-observer reliability.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Johns Hopkins Hospital In-Room Independence Scale
Time Frame: 1 week
The Johns Hopkins Hospital In-Room Independence Scale is a scale that assesses a person's in-room independence, assessing mobility, toileting, and cognition. It consists of 15 items. A person who passes all items receives a score of 15. Failure on any item indicates in-room dependency.
1 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morse Fall Scale
Time Frame: 1 week
The Morse Fall Scale is an 125-point assessment tool that evaluates the risk of falling by considering factors such as fall history, secondary diagnoses, need for a walking aid, gait and transfer, and mental status; higher scores indicate poorer functioning.
1 week
Hendrich II Fall Risk Scale
Time Frame: 1 week
The Hendrich II Fall Risk Scale assesses patients' fall risk. The scale includes factors like confusion, depression, dizziness, male gender, certain medications, and a mobility test. A score of 5 or above indicates high risk.
1 week
Barthel Index
Time Frame: 1 week
The Barthel Index is an evaluation tool used to measure independence in performing 10 physical activities of daily living, with a primary focus on self-care and mobility. Minimum: 0,. Maximum: 100 (higher is better).
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Banu Kuran, Professor, Sisli Hamidiye Etfal Training and Research Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2025

Primary Completion (Actual)

January 1, 2026

Study Completion (Actual)

January 15, 2026

Study Registration Dates

First Submitted

November 18, 2025

First Submitted That Met QC Criteria

November 18, 2025

First Posted (Actual)

November 26, 2025

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 25, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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