Study of Episodic Breathlessness in Patients With Lung Cancer or Other Advanced Disease
Primary Purpose
Dyspnea, Lung Cancer, Metastatic Cancer
Status
Completed
Phase
Locations
United Kingdom
Study Type
Observational
Intervention
medical chart review
study of socioeconomic and demographic variables
survey administration
quality-of-life assessment
Sponsored by
About this trial
This is an observational trial for Dyspnea focused on measuring dyspnea, lung metastases, recurrent non-small cell lung cancer, recurrent small cell lung cancer, extensive stage small cell lung cancer, stage IIIA non-small cell lung cancer, stage IIIB non-small cell lung cancer, stage IV non-small cell lung cancer
Eligibility Criteria
DISEASE CHARACTERISTICS:
Diagnosis of advanced disease as defined by the following criteria:
Lung cancer
- Primary lung cancer at all stages (small cell lung cancer [SCLC] and non-small cell lung cancer [NSCLC])
- Cancer at any site with secondary tumor of the lung (lung metastasis)
Chronic obstructive pulmonary disease (COPD)
- Stage III or IV of the Global Initiative for Obstructive Lung Disease (GOLD) classification, which includes the airflow limitation measured by spirometry FEV1 < 50%, FEV1/FVC < 0.7, and symptoms such as more severe breathlessness, reduced exercise capacity, and repeated exacerbations
Chronic heart failure (CHF)
- NYHA class II-IV heart disease, which includes symptoms such as dyspnea or palpitation and an increasing limitation of exercise capacity or discomfort at rest
Motor neuron disease (MND)
- All patients suffering from breathlessness
- Suffering from episodic breathlessness as defined above at any level of severity
PATIENT CHARACTERISTICS:
- Able to give informed consent
- Able to be interviewed
- No cognitive impairment (clinically judged by the principal investigator)
- No limited comprehension of the English language
PRIOR CONCURRENT THERAPY:
- Concurrent disease-oriented therapies (e.g., chemotherapy, radiotherapy, or surgery) allowed
Sites / Locations
- King's College Hospital
Outcomes
Primary Outcome Measures
Experiences of episodic breathlessness
Impact of episodic breathlessness on daily living
Individual coping strategies to reduce burden of episodic breathlessness
Secondary Outcome Measures
Full Information
NCT ID
NCT01138358
First Posted
June 4, 2010
Last Updated
August 23, 2013
Sponsor
King's College Hospital NHS Trust
1. Study Identification
Unique Protocol Identification Number
NCT01138358
Brief Title
Study of Episodic Breathlessness in Patients With Lung Cancer or Other Advanced Disease
Official Title
Experiences of Episodic Breathlessness (EB) in Patients With Advanced Disease
Study Type
Observational
2. Study Status
Record Verification Date
June 2010
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
August 2010 (Actual)
Study Completion Date
October 2012 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
King's College Hospital NHS Trust
4. Oversight
5. Study Description
Brief Summary
RATIONALE: Gathering information about experiences of episodic breathlessness in patients with advanced disease may help doctors learn more about the disease.
PURPOSE: This clinical trial is studying experiences of episodic breathlessness in patients with lung cancer or other advanced disease.
Detailed Description
OBJECTIVES:
To explore the experiences of episodic breathlessness in patients with advanced disease (i.e., primary and secondary lung cancer, chronic obstructive pulmonary disease [COPD], chronic heart failure [CHF], and motor neuron disease [MND]).
To explore the impact of episodic breathlessness on daily living.
To explore the individual coping strategies to reduce burden of episodic breathlessness.
OUTLINE: This is a multicenter study.
Patients undergo 1 to 2 interviews to collect data on experiences of breathlessness (in general, at rest, and on exertion including symptom description, interpretation, and meaning); experiences of episodic breathlessness (EB) (at rest and on exertion including symptom description, interpretation, meaning, and definition); trajectory/course of EB (onset/relief, time, and severity) and different types/trajectories of EB; impact of EB (burden, emotional reaction [panic and fear], care burden, and dependencies); triggers of EB (causes, situation, and settings) and predictability of EB; management of EB (coping strategies, non-pharmacological and pharmacological management [including different applications], worsen/relief, role of care in coping, and emotional/behavior strategies; views on and experiences with services/professionals in management of EB and response to professional advice; and attitudes towards the future, course of the disease, and awareness of prognosis. At the end of the interview, the patient will be asked to draw a figure that illustrates the trajectory of the episode. After the interview, a debriefing will be carried out to give the patient the chance to express worries, potential harm, or any comments about the interview. In addition to the interviews, further information will be collected including demographics, diagnosis and co-morbidities, current pharmacological and non-pharmacological treatments (medical history), functional status (Karnofsky), and breathlessness characteristics (e.g., intensity, frequency, and duration). The interviews will be tape-recorded, transcribed verbatim, and analyzed concurrently using Framework Approach.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspnea, Lung Cancer, Metastatic Cancer
Keywords
dyspnea, lung metastases, recurrent non-small cell lung cancer, recurrent small cell lung cancer, extensive stage small cell lung cancer, stage IIIA non-small cell lung cancer, stage IIIB non-small cell lung cancer, stage IV non-small cell lung cancer
7. Study Design
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
medical chart review
Intervention Type
Other
Intervention Name(s)
study of socioeconomic and demographic variables
Intervention Type
Other
Intervention Name(s)
survey administration
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Primary Outcome Measure Information:
Title
Experiences of episodic breathlessness
Title
Impact of episodic breathlessness on daily living
Title
Individual coping strategies to reduce burden of episodic breathlessness
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
Diagnosis of advanced disease as defined by the following criteria:
Lung cancer
Primary lung cancer at all stages (small cell lung cancer [SCLC] and non-small cell lung cancer [NSCLC])
Cancer at any site with secondary tumor of the lung (lung metastasis)
Chronic obstructive pulmonary disease (COPD)
Stage III or IV of the Global Initiative for Obstructive Lung Disease (GOLD) classification, which includes the airflow limitation measured by spirometry FEV1 < 50%, FEV1/FVC < 0.7, and symptoms such as more severe breathlessness, reduced exercise capacity, and repeated exacerbations
Chronic heart failure (CHF)
NYHA class II-IV heart disease, which includes symptoms such as dyspnea or palpitation and an increasing limitation of exercise capacity or discomfort at rest
Motor neuron disease (MND)
All patients suffering from breathlessness
Suffering from episodic breathlessness as defined above at any level of severity
PATIENT CHARACTERISTICS:
Able to give informed consent
Able to be interviewed
No cognitive impairment (clinically judged by the principal investigator)
No limited comprehension of the English language
PRIOR CONCURRENT THERAPY:
Concurrent disease-oriented therapies (e.g., chemotherapy, radiotherapy, or surgery) allowed
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steffen Simon, MD, MSC
Organizational Affiliation
King's College Hospital NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
King's College Hospital
City
London
State/Province
England
ZIP/Postal Code
SE5 9RJ
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
23094954
Citation
Simon ST, Niemand AM, Benalia H, Voltz R, Higginson IJ, Bausewein C. Acceptability and preferences of six different routes of drug application for acute breathlessness: a comparison study between the United Kingdom and Germany. J Palliat Med. 2012 Dec;15(12):1374-81. doi: 10.1089/jpm.2012.0249. Epub 2012 Oct 24.
Results Reference
derived
Learn more about this trial
Study of Episodic Breathlessness in Patients With Lung Cancer or Other Advanced Disease
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