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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