Management of Patients With Respiratory Symptoms in Sweden
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ClinicalTrials.gov Identifier: NCT02728674 |
Recruitment Status :
Completed
First Posted : April 5, 2016
Last Update Posted : August 24, 2017
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Chronic Obstructive Pulmonary Disease (COPD) | Other: Person in the case is a male. Other: Person in the case is a female. Other: Symptom in the case is breathlessness. Other: Symptom in the case is pain. | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 134 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
Primary Purpose: | Diagnostic |
Official Title: | Management of Patients With Respiratory Symptoms in Sweden |
Actual Study Start Date : | September 2016 |
Actual Primary Completion Date : | May 2017 |
Actual Study Completion Date : | May 2017 |

Arm | Intervention/treatment |
---|---|
Man+Breathlessness
Person in the case is a male. Symptom in the case is breathlessness.
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Other: Person in the case is a male.
Person in the case is a male. Other: Symptom in the case is breathlessness. Symptom in the case is breathlessness. |
Man+Pain
Person in the case is a male. Symptom in the case is pain.
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Other: Person in the case is a male.
Person in the case is a male. Other: Symptom in the case is pain. Symptom in the case is pain. |
Woman+Breathlessness
Person in the case is a female. Symptom in the case is breathlessness.
|
Other: Person in the case is a female.
Person in the case is a female. Other: Symptom in the case is breathlessness. Symptom in the case is breathlessness. |
Woman+Pain
Person in the case is a female.Symptom in the case is pain.
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Other: Person in the case is a female.
Person in the case is a female. Other: Symptom in the case is pain. Symptom in the case is pain. |
- COPD treatment in the Questionnaire [ Time Frame: through study completion, up to 6 months ]
Would there be a difference between the hypothetical case with breathlessness compared to the otherwise identical case with pain instead of breathlessness regarding:
- Proportion of study participants that consider that the patient in the case is not optimally treated;
- Proportion of study participants that consider morphine as either primary or secondary treatment option
- Gender bias in COPD diagnosis in the Questionnaire [ Time Frame: through study completion, up to 6 months ]
Would there be a difference between the cases with a male respective female patient regarding:
- Proportion of study participants that consider COPD diagnosis;
- Proportion of study participants that consider spirometry for further diagnostics
- Symptomatic treatment in the Questionnaire [ Time Frame: through study completion, up to 6 months ]
Would there be a difference between the case with breathlessness compared with the case with pain regarding:
- Chosen treatment options;
- Reasons not to choose treatment with opioids Chosen treatment options Reasons not to choose treatment with opioids
- Non-randomized measurements in the Questionnaire [ Time Frame: through study completion, up to 6 months ]Proportion of study participants that consider the described breathlessness to be refractory
- Chosen evidence-grades as non-randomized measurements in the Questionnaire [ Time Frame: through study completion, up to 6 months ]Chosen evidence-grades for treatment options of refractory breathlessness
- Chosen potential risks as non-randomized measurements in the Questionnaire [ Time Frame: through study completion, up to 6 months ]Chosen potential risks with opioid treatment

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria (all required):
- Certified physician
- Treats patients with respiratory symptoms and reduced physical activity
- Able to read and understand a hypothetical case in Swedish
Exclusion Criteria:
- Knowledge about the aim and/or design of the study, or
- Previous participation in the study

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02728674
Sweden | |
Department of Respiratory Medicine and Allergology | |
Lund, Skane, Sweden, 21100 |
Principal Investigator: | Magnus Ekström, MD, PhD | Department of Medicine, Blekinge Hospital, SE-37185 Karlskrona |
Responsible Party: | Magnus Ekström, MD, PhD, Skane University Hospital |
ClinicalTrials.gov Identifier: | NCT02728674 |
Other Study ID Numbers: |
CASE2016 |
First Posted: | April 5, 2016 Key Record Dates |
Last Update Posted: | August 24, 2017 |
Last Verified: | August 2017 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
COPD Breathlessness Symptom Opioids Gender bias |
Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive Signs and Symptoms, Respiratory Lung Diseases |
Respiratory Tract Diseases Chronic Disease Disease Attributes Pathologic Processes |