NCT07119099

Brief Summary

The primary aim of our study was to investigate the relationship between 6PBRT outcome measures and 6MWT, 1MSTST and UULEX outcome measures. The secondary aim is to investigate the predictors of 6PBRT test.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
21

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2025

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

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

First Submitted

Initial submission to the registry

July 30, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

August 4, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

August 12, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 13, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 26, 2025

Completed
Last Updated

March 3, 2026

Status Verified

March 1, 2026

Enrollment Period

2 months

First QC Date

July 30, 2025

Last Update Submit

March 2, 2026

Conditions

Keywords

6-minute pegboard and ring testupper extremityexercise capacityidiopathic pulmonary fibrosis

Outcome Measures

Primary Outcomes (4)

  • 1 Minute Sit to Stand Test (1MSTST)

    The 1-Minute Sit-to-Stand Test (1MSTST) is a simple, inexpensive, and practical assessment used to evaluate functional capacity in a small space. During the test, participants are asked to repeatedly sit down and stand up from a fixed chair as quickly as possible for one minute, without using their arms for support.

    Day 1

  • Unsupported Upper-Limb Exercise Test (UULEX)

    Patients will be instructed to lift five bars consecutively and rhythmically until the onset of fatigue. The bars will have incremental weights of 200 g, 500 g, 1 kg, and 2 kg, respectively. The duration of the activity will be recorded to assess the patients' endurance levels.

    Day 1

  • 6 Minutes Pegboard and Ring Test (6PBRT)

    The 6-Minute Pegboard and Ring Test (6PBRT) is designed to assess upper extremity functional capacity using unsupported arm movements. The setup includes four horizontally aligned bars: two at shoulder height and two positioned 20 cm above. Participants, seated with back support, sequentially transfer rings between the bars for six minutes, and the total number of rings moved serves as the performance score.

    Day 1

  • 6 Minutes Walking Tests (6MWT)

    Total distance walked (in meters) during the 6MWT will be recorded. Higher distance reflects improved functional capacity.

    Day 1

Secondary Outcomes (8)

  • Spirometric measurements (Forced vital capacity - FVC)

    Day 1

  • Spirometric measurements (First second forced expiratory volume - FEV1)

    Day 1

  • Spirometric measurements (FEV1/FVC ratio)

    Day 1

  • Carbon monoxide diffusion capacity

    Day 1

  • Modified Medical Research Council Dyspnea Score

    Day 1

  • +3 more secondary outcomes

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Chest Diseases Clinic of Süreyyapaşa Chest Diseases and Thoracic Surgery Training and Research Hospital

You may qualify if:

  • Our study included subjects who were diagnosed with IPF according to the ATS/ERS/JRS/ALAT guidelines, were over 18 years of age, had not changed their treatment for the last 3 months, and had a stable clinical status for the last 3 months.

You may not qualify if:

  • Subjects with orthopedic comorbidity affecting upper extremity use, neurologic comorbidity, severe postural impairment, uncontrolled cardiac or cardiometabolic comorbidity, newly diagnosed cancer, obstructive pulmonary disease, recent surgery and those who refused to volunteer were excluded.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Süreyyapaşa Chest Diseases and Thoracic Surgery Training and Research Hospital

Istanbul, Turkey (Türkiye)

Location

Süreyyapaşa

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Idiopathic Pulmonary Fibrosis

Condition Hierarchy (Ancestors)

Pulmonary FibrosisLung Diseases, InterstitialLung DiseasesRespiratory Tract Diseases

Study Officials

  • Anıl Gökçen, Phsiotheraphist

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist

Study Record Dates

First Submitted

July 30, 2025

First Posted

August 12, 2025

Study Start

August 4, 2025

Primary Completion

October 13, 2025

Study Completion

December 26, 2025

Last Updated

March 3, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations