- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03881046
Multidimensional Evaluation Of Daily Living Activities And Quality Of Life In Lung Cancer Patients
Multidimensional Evaluation Of Daily Living Activities And Quality Of Life In Lung Cancer
Study Overview
Status
Conditions
Detailed Description
Lung cancer is the abnormal proliferation of cells in the lung tissue and a mass in the lung. The primary symptoms of this health problem include cough, dyspnea, chest pain, hemoptysis and sputum. In addition to these symptoms, muscle strength, respiratory function and effort level are decreased.
Inadequate daily living activities in cancer patients are expressed.But studies evaluating the activities of daily living in patients with lung cancer are inadequate and patients are evaluated only using scales. For the measurement of functional status in daily living activities, these scales provide important information about the detection of symptoms and the progression of the disease. However, it is very difficult to determine the limitation of perceived difficulty in daily living activities with these scales. In addition, since these scales are a method of measurement, the objectivity is open to discussion. It is thought that a performance-based protocol will facilitate the detection of limitations and provide more objective findings. We think that the Londrina protocol fully reflects the activities of daily living and thus will give us an objective measurement.
This study will show us the problem and its cause in daily life activities in patients with lung cancer.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ankara, Turkey, 06105
- Hamide Sahin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- To have a diagnosis of lung cancer
- Complete chemotherapy
- Complete radiotherapy
- Coopere,
- Accepts participation in the study will be included in the study
Exclusion Criteria:
- Neurological, cognitive or orthopedic diseases that affect the measurements
- Acute infection
- Individuals with other chronic diseases that may affect their walking will not be included in the study
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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healthy control group
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lung cancer
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Activities Of Daily Living
Time Frame: 1st day
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Daily Living Activities will be evaluated using the Londrina Protocol.The protocol consists of 5 stations.
Stations are including organizing books on the table, 18 meters walking by carrying 10% of body weight symmetrically, arranging books by putting them on shelves, hanging the laundry in the laundry basket and walking 18 meters.
İndividual will do these activities at his own pace and the time will be recorded at the end.
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1st day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Life Quality
Time Frame: 1st Day
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Quality of life will be measured using Core Quality of Life Questionnaire (EORTC QLQ-C30) The questionnaire consists of 30 questions and provides information on quality of life and symptoms.
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1st Day
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Peripheral Muscle Strength
Time Frame: 1st Day
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Muscle strength will be evaluated by force measuring dynamometer device 3 times.
M.Quadriceps Femoris, shoulder abduction, shoulder flexion, elbow flexion, elbow extension and hand grip strength of all cases will be measured.
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1st Day
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Dyspnoea
Time Frame: 1st Day
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Dyspnoea will be evaluated using the Medical Research Council Dyspnoea Scale.
The Medical Research Council Dyspnoea Scale has a score of 0-4.
İn this scoring system 0 indicates that there is no dyspnoea, whereas 4 indicates that the dyspnoea is too high.
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1st Day
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Respiratory Functions
Time Frame: 1st Day
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Respiratory functions will be measured by spirometric measurement.
This measurement will give us FEV1 FVC FEV1 / FVC values.
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1st Day
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Exercise Capacity
Time Frame: 1st Day
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6 Minute walk test will be used.In the test, the person will be asked to walk as fast as possible in a 30-meter corridor and the walking distance will be recorded in 6 minutes.
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1st Day
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO 18/737-08
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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