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临床试验/NCT07122141
NCT07122141进行中(未招募)不适用

Validity and Reliability of the 6-Minute Pegboard and Ring Test in Interstitial Lung Disease

Marmara University1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2025年4月25日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
27
试验地点
1
主要终点
6 Minutes Pegboard and Ring Test (6PBRT)

研究概览

简要总结

The aim of this study is to investigate the validity and reliability of the 6 Minutes Pegboard and Ring Test (6PBRT) in patients with Interstitial Lung Disease (ILD).

详细描述

Our study was conducted in the Chest Diseases Clinic of Süreyyapaşa Chest Diseases and Thoracic Surgery Training and Research Hospital. Our study was approved by the Marmara University Faculty of Health Sciences Non-Interventional Clinical Research Ethics Committee and was conducted in accordance with the Declaration of Helsinki. Signed informed consent was obtained from the participants.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • Neurological comorbidity,
  • Orthopedic comorbidity that impairs upper extremity function,
  • Kyphoscoliosis and/or severe postural abnormalities,
  • Uncontrolled cardiac problems,
  • Uncontrolled diagnosis of Diabetes Mellitus,
  • Ischemic heart disease,
  • Newly diagnosed history of cancer,
  • Diagnosis of obstructive pulmonary disease,
  • Cognitive impairments such as Alzheimer's or dementia,
  • Use of immunosuppressive medications (excluding corticosteroids),
  • History of recent surgery,
  • Refusal to answer questions,
  • Refusal to participate voluntarily.

结局指标

主要结局

6 Minutes Pegboard and Ring Test (6PBRT)

时间窗: Day 1

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.

6 Minutes Walking Tests (6MWT)

时间窗: Day 1

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

Unsupported Upper-Limb Exercise Test (UULEX)

时间窗: Day 1

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.

次要结局

  • 1 Minute Sit to Stand Test (1MSTST)(Day 1)
  • 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)
  • Gender-Age-Physiology (GAP) Index(Day 1)
  • Modified Medical Research Council Dyspnea Score(Day 1)
  • Handgrip Strength(Day 1)
  • Fatigue severity scale(Day 1)
  • London Chest Daily Activities of Living Scale(Day 1)
  • Saint George Quality of life questionnaire(Day 1)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anıl Gökçen

Physiotherapist

Marmara University

研究点 (1)

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