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NCT06922292

"Turkish Validation of the Respiratory Distress Observation Scale in Palliative Care"

Completed Last updated 10 February 2026
What this trial tests

trial in Dyspnea in 100 participants. Completed in 30 May 2025.

Timeline
1 February 2025
Primary endpoint
20 May 2025
30 May 2025

Quick facts

Lead sponsorIstinye University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date1 February 2025
Primary completion20 May 2025
Estimated completion30 May 2025
Sites1 location across Turkey (Türkiye)

Conditions studied

Sponsor

Istinye University

Who can join

18 and older, any sex, with Dyspnea or Palliative Care. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Dyspnea is a subjective experience influenced by physiological, cognitive, behavioral, and sociocultural factors. While self-reported scales are commonly used to assess dyspnea severity, they are unsuitable for patients unable to communicate, such as those with cognitive impairment or sedation. The Respiratory Distress Observation Scale (RDOS), developed by Campbell in 2008, is a reliable and valid tool for evaluating dyspnea in non-communicative palliative care patients. The RDOS has been adapted into Chinese and Italian, but a Turkish version is lacking. This study aims to assess the reliability and validity of the Turkish version of the RDOS.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Dyspnea

Currently open trials in the same condition.

Other Istinye University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06922292.

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