Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
61 participants
INTERVENTIONAL
2023-04-01
2024-06-30
Brief Summary
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Detailed Description
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Method: The research was planned as a randomized, controlled experimental design. The population of the research consists of patients treated with a diagnosis of COPD in Bartın State Hospital Chest Diseases Service. Considering the data obtained from a similar study, the sample was calculated as 64 patients in the intervention group and 64 patients in the control group, for a total of 128 patients. Data will be collected using the Descriptive Information Form, Vital Signs Form, Modified Borg Scale, and Saint George Respiratory Questionnaire.
Data will be collected by researchers through face-to-face interviews with COPD patients treated at Bartın State Hospital Chest Diseases Service. Patients receiving treatment with a diagnosis of COPD will be randomized into intervention and control groups. In the control group, the Patient Diagnosis Form, Vital Signs Form, Modified Borg Scale, and Saint George Respiratory Questionnaire Form will be filled in at the first interview. The clinic's routine care protocol will be applied to the patients in the control group, and the researchers will fill out a vital signs form every day for 7 days, and the patients will be followed up. At the first meeting of the intervention group, the Patient Identification Form, Vital Signs Form, Modified Borg Scale, and Saint George Respiratory Questionnaire Form will be filled out. Afterward, training will be given (accompanied by an academic advisor) on how to apply cold air to the face with a hand fan (3 times a day for 5 minutes) for dyspnea management. Additionally, patients will be given a hand-fan application brochure. The researchers will monitor the patient every day for a week (7 days), fill out the vital signs form, and the final test will be administered by the researchers on the 8th day.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Hand-fan application to the face
At the first meeting of the hand-fan application to the face group, the Patient Identification Form, Vital Signs Form, Modified Borg Scale, and Saint George Respiratory Questionnaire Form will be filled out. Afterward, training will be given (accompanied by an academic advisor) on how to apply cold air to the face with a hand fan (3 times a day for 5 minutes) for dyspnea management. Additionally, patients will be given a hand-fan application brochure. The researchers will monitor the patient every day for a week (7 days), fill out the vital signs form, and the final test will be administered by the researchers on the 8th day.
Hand-fan application to the face
Hand fan application is one of the applications recommended in managing dyspnea in evidence-based guidelines. Hand fan application effectively reduces shortness of breath by stimulating cold airflow to the 2nd and 3rd trigeminal nerve branches, mucosa, and skin.
Standard care group
In the standard care group, the Patient Diagnosis Form, Vital Signs Form, Modified Borg Scale, and Saint George Respiratory Questionnaire Form will be filled in at the first interview. The clinic's routine care protocol will be applied to the patients in the control group, and the researchers will fill out a vital signs form every day for a week, and the patients will be followed up.
No interventions assigned to this group
Interventions
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Hand-fan application to the face
Hand fan application is one of the applications recommended in managing dyspnea in evidence-based guidelines. Hand fan application effectively reduces shortness of breath by stimulating cold airflow to the 2nd and 3rd trigeminal nerve branches, mucosa, and skin.
Eligibility Criteria
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Inclusion Criteria
* Being over 18 years of age,
* No open wounds on the face for any reason,
* Lung cancer, tuberculosis, asthma etc. absence of other respiratory system diseases,
* Not having a hearing or speech impairment,
* Not having a cognitive disability
* Volunteering to participate in the research.
Exclusion Criteria
* Being under 18 years of age,
* Having an open wound on the face for any reason,
* Lung cancer, tuberculosis, asthma etc. Having other respiratory system diseases,
* Having hearing and speech impairment,
* Having a cognitive disability
* Not volunteering to participate in the research.
18 Years
ALL
No
Sponsors
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The Scientific and Technological Research Council of Turkey
OTHER
Bartın Unıversity
OTHER
Responsible Party
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Necmiye ÇÖMLEKÇİ
Research Assistant, PhD
Locations
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Necmiye ÇÖMLEKÇİ
Bartın, , Turkey (Türkiye)
Countries
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Other Identifiers
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BU-FHS-NC-03
Identifier Type: -
Identifier Source: org_study_id
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