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Trial Title: Active Cycle of Breathing Techniques on Respiratory Distress Symptom Cluster

NCT ID: NCT05879354

Condition: Lung Neoplasms

Conditions: Official terms:
Lung Neoplasms
Syndrome

Conditions: Keywords:
Active Cycle of Breathing Techniques
Lung Neoplasms
Symptom Cluster
Nursing
Care

Study type: Interventional

Study phase: N/A

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Intervention model description: The intervention group will apply the Active Cycle of Breathing Techniques with video twice a day for 28 days and the control group will not.

Primary purpose: Supportive Care

Masking: None (Open Label)

Intervention:

Intervention type: Other
Intervention name: Active Cycle of Breathing Techniques
Description: Patients in the intervention group will be provided with video-guided Active Cycle of Breathing Techniques twice a day for 28 days.
Arm group label: Active Cycle Of Breathing Techniques Group

Summary: This study was designed as a randomized, control group, experimental study to examine the effect of Active Cycle of Breathing Techniques application on respiratory distress symptom cluster in patients with lung cancer.

Detailed description: The sample of the study will consist of patients who received chemotherapy treatment with the diagnosis of Stage IV non-small cell lung cancer in the outpatient chemotherapy service of a training and research hospital and met the inclusion criteria. Data in the study will be collected using the Patient Information Form, Eastern Cooperative Oncology Group (ECOG) Performance Scale, Cancer Dyspnea Scale, Leicester Cough Questionnaire and Cancer Fatigue Scale. In order to test the applicability and comprehensibility of the forms to be used before the study, a preliminary application will be made with 5 patients. This study is planned to prepare a video describing the application for patients to use while performing the Active Cycle of Breathing Techniques application. On the 1st day of the study, a 10-minute face-to-face training will be given to the intervention (experimental) group by the researcher using the video about the Active Cycle of Breathing Techniques. In the research, the intervention (experimental) group will be asked to follow the video to be prepared and apply the Active Cycle of Breathing Techniques twice a day for 28 days. The intervention (experimental) group will be monitored by telephone call once a week and 3 times using the Patient Follow-up Form (days 7, 14 and 21). On the other hand, only the pre-test and post-test will be applied to the control group.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Being 18 years or older - Being diagnosed with stage IV non-small cell lung cancer - Being diagnosed with lung cancer in the type of adenocarcinoma and squamous cell carcinoma - Receiving outpatient chemotherapy treatment - Receiving the first course of chemotherapy treatment - ECOG Performance Scale Score < 3 - Having all the symptoms of dyspnea, cough, and fatigue - Not having a cognitive disorder or a diagnosed psychiatric illness - Being able to speak Turkish - Volunteering to participate in the research Exclusion Criteria: - Experiencing a chronic obstructive pulmonary disease (COPD) exacerbation in the last 4 weeks - Having an active lung infection - Not volunteering to participate in the research - Not having dyspnea, cough, and fatigue symptoms - Not speaking Turkish

Gender: All

Minimum age: 18 Years

Maximum age: 80 Years

Healthy volunteers: No

Start date: June 10, 2023

Completion date: May 30, 2024

Lead sponsor:
Agency: Maltepe University
Agency class: Other

Collaborator:
Agency: Saglik Bilimleri Universitesi
Agency class: Other

Source: Maltepe University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05879354

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