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Cognitive and Behavioral Intervention for the Management of Episodic Breathlessness in Patients With Advanced Disease (CoBeMEB)

Primary Purpose

Dyspnea, Respiratory Insufficiency, Neoplasms

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Cognitive and Behavioral intervention for the Management of Episodic Breathlessness
Sponsored by
University of Cologne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Dyspnea focused on measuring Clinical Trial, Phase II, Cognitive Behavioral Therapy, Feasibility Studies

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • In- and outpatients of the participating centers with episodic breathlessness due to a life-limiting progressive disease
  • Recurrent breathlessness episodes despite optimal treatment of the underlying disease
  • Eastern Cooperative Oncology Group (ECOG) status 0-3
  • Estimated life-expectancy should be at least 8 weeks as judged by the treating physician
  • Ability to understand, read, and respond to German language
  • Informed consent

Exclusion Criteria:

  • Episodic breathlessness due to reversible and treatable causes, such as acute pneumonia, pulmonary embolism, chronic hyperventilation syndrome, asthma or other reversible or unknown cause
  • Cognitive impairment
  • Severe current health impairments that do not allow participation after clinical evaluation by the treating physician

Sites / Locations

  • University Hospital of Cologne

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Cognitive and Behavioral Intervention

Arm Description

Non-pharmacological strategies for the Management of episodic breathlessness

Outcomes

Primary Outcome Measures

Enrollment rate (Feasibility)
Ratio of patients screened and patients that signed informed consent
Study completion rate (Feasibility)
Ratio of patients who signed the informed consent and filled out the final assessment
Drop Outs (Feasibility)
Withdrawal from the study at specific date (e.g. Intervention, refresher, Outcome at week 2/4/6)

Secondary Outcome Measures

Occurence of side-effects due to the brief cognitive and behavioral Intervention (Safety)
closed-ended question (yes/no)
Occurence of adverse events due to the brief cognitive and behavioral Intervention (Safety)
closed-ended Question (yes/no)
Occurence of adverse events due to the study procedure (Safety)
closed-ended Question (yes/no)
Satisfaction with the brief cognitive and behavioral intervention (Acceptability)
closed-ended Questions
Patients' experience with the Intervention and study procedure
qualitative interview
Potential effects of the brief cognitive and behavioral Intervention on Depression
Hospital Anxiety and Depression Scale: the Depression Subscale (the higher the score, the worse the outcome)
Potential effects of the brief cognitive and behavioral Intervention on Anxiety
Hospital Anxiety and Depression Scale: the Anxiety Subscale (the higher the score, the worse the outcome)
Potential effects of the brief cognitive and behavioral Intervention on breathlessness mastery
Mastery Domain of the Chronic Respiratory Questionnaire (the higher the score, the better the outcome)
Potential effects of the brief cognitive and behavioral Intervention on Quality of Life
Chronic Respiratory Questionnaire (the higher the score, the better the outcome)
Potential effects of the brief cognitive and behavioral Intervention on Palliative Care needs
Integrated Palliative Care Outcome Scale (the higher the score, the worse the outcome)
Potential effects of the brief cognitive and behavioral Intervention on catastrophizing thoughts concerning dyspnea
Dyspnea catastrophizing scale (the higher the score, the worse the outcome)
Informal caregivers' burdens while caring for breathlessness patients
Zarid Burden Interview (the higher the score, the worse the Outcome)
Informal caregivers' experience with Intervention and study procedure
qualitative interview

Full Information

First Posted
November 6, 2020
Last Updated
November 13, 2020
Sponsor
University of Cologne
Collaborators
University Hospital of Cologne, Bethanien Krankenhaus gGmbH
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1. Study Identification

Unique Protocol Identification Number
NCT04630743
Brief Title
Cognitive and Behavioral Intervention for the Management of Episodic Breathlessness in Patients With Advanced Disease
Acronym
CoBeMEB
Official Title
Cognitive and Behavioral Intervention for the Management of Episodic Breathlessness in Patients With Advanced Disease: a Single-arm Therapeutic Exploratory Trial (Phase II)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
February 9, 2019 (Actual)
Primary Completion Date
March 1, 2020 (Actual)
Study Completion Date
March 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cologne
Collaborators
University Hospital of Cologne, Bethanien Krankenhaus gGmbH

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Episodic breathlessness is a common and distressing symptom in patients with advanced disease such as cancer, chronic obstructive pulmonary disease (COPD) and chronic heart failure. Since the short duration of the majority of breathless episodes limits the effectiveness of pharmacological interventions (e.g. opioids), non-pharmacological management strategies play a major role. As non-pharmacological strategies patients use, for example, cognitive and behavioural methods such as breathing or relaxation techniques. The aim of the study is to test a brief cognitive and behavioural intervention for an improved management of episodic breathlessness. Initially, a Delphi procedure with international experts has been used to develop the brief intervention consisting of various non-pharmacological strategies to enhance the management of breathless episodes. In the single-arm therapeutic exploratory trial (phase II), the feasibility and potential effects of the brief intervention, such as patient-reported breathlessness mastery, episodic breathlessness characteristics, quality of life, symptom burden, caregivers' burden, and breathlessness in general will be examined. The results of the study form the basis for planning and implementing a subsequent confirmatory randomized control trial (phase III).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspnea, Respiratory Insufficiency, Neoplasms, Pulmonary Disease, Chronic Obstructive, Lung Diseases, Heart Failure, Lung Diseases, Interstitial, Palliative Care, Palliative Medicine, Breathlessness
Keywords
Clinical Trial, Phase II, Cognitive Behavioral Therapy, Feasibility Studies

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
single-arm therapeutic exploratory trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive and Behavioral Intervention
Arm Type
Other
Arm Description
Non-pharmacological strategies for the Management of episodic breathlessness
Intervention Type
Behavioral
Intervention Name(s)
Cognitive and Behavioral intervention for the Management of Episodic Breathlessness
Intervention Description
The cognitive and behavioral brief intervention comprises two parts: In a first module, the intervention and the study team is introduced, the definition of episodic breathlessness is given and the individual characteristics of breathlessness episodes are recorded. Goals of the intervention are discussed. In a subsequent module on patient education and the strategies, the patient and intervention executor discuss the patients' assumptions about episodic breathlessness including triggers and already used management strategies for breathlessness episodes. This follows the presentation of the non-pharmacological strategies: movement of air/ handheld fan, forward lean, diaphragmatic breathing, distraction, pursed lips breathing, long breaths out and relaxation training. The patient selects 2-3 strategies and trains them with the intervention executor.
Primary Outcome Measure Information:
Title
Enrollment rate (Feasibility)
Description
Ratio of patients screened and patients that signed informed consent
Time Frame
week 6
Title
Study completion rate (Feasibility)
Description
Ratio of patients who signed the informed consent and filled out the final assessment
Time Frame
week 6
Title
Drop Outs (Feasibility)
Description
Withdrawal from the study at specific date (e.g. Intervention, refresher, Outcome at week 2/4/6)
Time Frame
week 6
Secondary Outcome Measure Information:
Title
Occurence of side-effects due to the brief cognitive and behavioral Intervention (Safety)
Description
closed-ended question (yes/no)
Time Frame
week 6
Title
Occurence of adverse events due to the brief cognitive and behavioral Intervention (Safety)
Description
closed-ended Question (yes/no)
Time Frame
week 6
Title
Occurence of adverse events due to the study procedure (Safety)
Description
closed-ended Question (yes/no)
Time Frame
week 6
Title
Satisfaction with the brief cognitive and behavioral intervention (Acceptability)
Description
closed-ended Questions
Time Frame
week 6
Title
Patients' experience with the Intervention and study procedure
Description
qualitative interview
Time Frame
week 6
Title
Potential effects of the brief cognitive and behavioral Intervention on Depression
Description
Hospital Anxiety and Depression Scale: the Depression Subscale (the higher the score, the worse the outcome)
Time Frame
week 2, 4 and 6
Title
Potential effects of the brief cognitive and behavioral Intervention on Anxiety
Description
Hospital Anxiety and Depression Scale: the Anxiety Subscale (the higher the score, the worse the outcome)
Time Frame
week 2, 4 and 6
Title
Potential effects of the brief cognitive and behavioral Intervention on breathlessness mastery
Description
Mastery Domain of the Chronic Respiratory Questionnaire (the higher the score, the better the outcome)
Time Frame
week 2, 4 and 6
Title
Potential effects of the brief cognitive and behavioral Intervention on Quality of Life
Description
Chronic Respiratory Questionnaire (the higher the score, the better the outcome)
Time Frame
week 2, 4 and 6
Title
Potential effects of the brief cognitive and behavioral Intervention on Palliative Care needs
Description
Integrated Palliative Care Outcome Scale (the higher the score, the worse the outcome)
Time Frame
week 2, 4 and 6
Title
Potential effects of the brief cognitive and behavioral Intervention on catastrophizing thoughts concerning dyspnea
Description
Dyspnea catastrophizing scale (the higher the score, the worse the outcome)
Time Frame
week 2, 4 and 6
Title
Informal caregivers' burdens while caring for breathlessness patients
Description
Zarid Burden Interview (the higher the score, the worse the Outcome)
Time Frame
week 2, 4 and 6
Title
Informal caregivers' experience with Intervention and study procedure
Description
qualitative interview
Time Frame
week 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: In- and outpatients of the participating centers with episodic breathlessness due to a life-limiting progressive disease Recurrent breathlessness episodes despite optimal treatment of the underlying disease Eastern Cooperative Oncology Group (ECOG) status 0-3 Estimated life-expectancy should be at least 8 weeks as judged by the treating physician Ability to understand, read, and respond to German language Informed consent Exclusion Criteria: Episodic breathlessness due to reversible and treatable causes, such as acute pneumonia, pulmonary embolism, chronic hyperventilation syndrome, asthma or other reversible or unknown cause Cognitive impairment Severe current health impairments that do not allow participation after clinical evaluation by the treating physician
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steffen Simon, Prof., M.Sc.
Organizational Affiliation
Center of palliative medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Cologne
City
Cologne
State/Province
NRW
ZIP/Postal Code
50937
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

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Cognitive and Behavioral Intervention for the Management of Episodic Breathlessness in Patients With Advanced Disease

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