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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06286072
Other study ID # YCEYHANS
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date March 30, 2024

Study information

Verified date February 2024
Source Kirsehir Ahi Evran Universitesi
Contact Yasemin CEYHAN
Phone +905464589806
Email yasemin-ceyhan@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

COPD is an important respiratory system disease that progresses with damage to the airways.Increased mucus secretion and thickening in the airways causes obstruction.This obstruction causes symptoms such as shortness of breath, cough, phlegm and wheezing.The most obvious problem that the emerging symptoms will cause for the patient is fatigue.Coping with fatigue is an important problem in COPD. The main questions it aims to answer are: 1. Does the training given in COPD affect the level of fatigue? 2. Do the education given and text messages sent regarding COPD affect the level of fatigue? In this study, patients were given informative education about COPD and ways to cope with fatigue were explained. Then, in order to increase the permanence of the training, motivational messages and short briefings were continued for 8 weeks.2 messages were sent per week. Three groups were created to reveal the effectiveness of the trainings and messages. Group 1 was trained and messages were sent for 8 weeks. Group 2 was trained and no message was sent. Group 3 is the control group. No training has been provided other than routine maintenance. The initial information of all groups was taken again at the end of the 8th week. Main outcomes: - Dyspnea severity, - COPD general conditions and - Fatigue level. The results obtained will be interpreted by comparing between 3 groups.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date March 30, 2024
Est. primary completion date January 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Diagnosed with COPD for the last 1 year - Hospitalized for at least 3 days, - Voluntary patients Exclusion Criteria: - Under 18 years old - Over 85 years old - Those with chronic fatigue syndrome - Those with severe heart failure - Those who had surgery in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Education and message
COPD general education content and fatigue-specific coping strategies. Messages sent to phones

Locations

Country Name City State
Turkey Yasemin CEYHAN Kirsehir Center

Sponsors (1)

Lead Sponsor Collaborator
Kirsehir Ahi Evran Universitesi

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fatigue Level Evaluated with COPD ASTHMA FATIGUE SCALE. Applied at baseline and after 8 weeks.
Primary Dyspnea Severity Evaluated with mMRC Dyspnea Scale Applied at baseline and after 8 weeks.
Secondary COPD general condition Evaluated with COPD ASSESSMENT QUESTIONNAIRE (CAT) Applied at baseline and after 8 weeks.
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