Active Cycle of Breathing Techniques on Respiratory Distress Symptom Cluster

Maltepe University

Status

Completed

Conditions

Lung Neoplasms

Treatments

Other: Active Cycle of Breathing Techniques

Study type

Interventional

Funder types

Other

Identifiers

NCT05879354

MAU_DogaUlcay_001

Details and patient eligibility

About

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.

Full 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.

Enrollment

78 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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