Londrina Activities of Daily Living Protocol in Idiopathic Pulmonary Fibrosis Patients

NCT06049004 | Completed

• 1 other identifier: IKC124
• Study Type: observational
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

The Londrina Activities of Daily Living Protocol was first developed for Chronic Obstructive Pulmonary Disease patients and was found to be valid and reliable, but there is no validity and reliability study of the Londrina Activities of Daily Living Protocol in IPF patients. The purpose of the study is to Examine the Validity and Reliability of the Londrina Activities of Daily Living Protocol in Idiopathic Pulmonary Fibrosis (IPF) patients.

Conditions

Idiopathic Pulmonary Fibrosis; Activity, Motor

Keywords

idiopathic pulmonary fibrosis; activity daily living; validity; reliability

Outcome Measures

Primary Outcomes (1)

• Londrina Activities of Daily Living Protocol

  The protocol is a performance-based objective measurement method based on repetition of daily activities. Participants are asked to perform the activities defined in the protocol at the same speed they do at home. The Londrina Protocol includes 5 stations: Station 1 Arranging Objects on the Table, Station 2 Walking with Bags, Station 3 Organizing Shelves, Station 4 Clothesline Task, Station 5 Walking. The completion time of the protocol is recorded.

  15 minutes

Secondary Outcomes (5)

• Glittre Activities of Daily Living Test:

  5 minutes

• London Chest Activities of Daily Living (ADL) Scale

  10 minutes

• Hand Grip Strength Measurement

  5 minutes

• mMRC Dyspnea Scale

  5 minutes

• Respiratory Function Test

  10 minutes

Interventions

Activities of Daily Living Protocol OTHER

The protocol is a performance-based objective measurement method based on repetition of daily activities. Participants are asked to perform the activities defined in the protocol at the same speed they do at home. The Londrina Protocol includes 5 stations: Station 1 Arranging Objects on the Table, Station 2 Walking with Bags, Station 3 Organizing Shelves, Station 4 Clothesline Task, Station 5 Walking. The completion time of the protocol is recorded.

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients being diagnosed with idiopathic pulmonary fibrosis (IPF) disease

You may qualify if:

• Being diagnosed with idiopathic pulmonary fibrosis (IPF) disease
• Being 18 years or older
• Being independent in daily living activities
• Being able to read and understand Turkish

You may not qualify if:

• The patient refuses to participate in the study
• People with comorbidities that would make it impossible to perform any of the study evaluations (orthopedic pathology, uncontrolled cardiovascular or neurological conditions, psychiatric illness, etc.)
• Presence of infection in the last 3 months
• Those who show changes in their usual symptoms during the protocol
• Patients who have difficulty understanding the commands given
• Those who cannot complete all evaluations

Sponsors & Collaborators

• Izmir Katip Celebi University: lead

Study Sites (1)

Izmir Katip Celebi University

Izmir, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Idiopathic Pulmonary Fibrosis; Motor Activity

Condition Hierarchy (Ancestors)

Pulmonary Fibrosis; Lung Diseases, Interstitial; Lung Diseases; Respiratory Tract Diseases; Behavior

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: OTHER
• Target Duration: 1 Week
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assoc. Prof.

Study Record Dates

• First Submitted: September 15, 2023
• First Posted: September 21, 2023
• Study Start: November 1, 2023
• Primary Completion: June 1, 2024
• Study Completion: November 1, 2024
• Last Updated: June 5, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)