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OpenTrials
Completed

NCT Number: NCT04305639

The Reliability and Validity of Turkish Version of ''The Dyspnea-ALS-Scale (DALS-15)"

The Dyspnea-ALS-Scale (DALS-15) is a uni-dimensional scale to measure dyspnea in patients with Amyotrophic Lateral Sclerosis. It can be easily and rapidly applied. The aim of this study is to investigate reliability and validity of Turkish version of the DALS-15.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age of 18 or above
  • Dyspnea on exertion, dyspnea at rest, or orthopnea without evidence of pulmonary or cardiac causes of dyspnea

Exclusion criteria

  • Severe cognitive dysfunction

Treatment and study plan

Primary outcomes

  1. The Dyspnea-ALS-Scale (DALS-15)

    Time frame: 10 minutes

    The scale is used to measure dyspnea in ALS patients

Secondary outcomes

  1. Modified Borg Scale

    Time frame: 10 minutes

    A 10 point Modified Borg Scale is used to assess dyspnea in supine and standing positions.

  2. Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R)

    Time frame: 15 minutes

    It is used to assess functional stats in ALS patients. This study particularly focus on pulmonary functions and dyspnea subscale of the scale.

Sponsors and collaborators

Lead sponsor

Istanbul Medeniyet University

Other

Collaborators

  • Istanbul University
  • Istanbul University - Cerrahpasa

Registry information

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Mar 12, 2020
Registry last updated
Apr 9, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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