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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, average 1 year
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to test a non-drug therapy to help adults with ILD manage their chronic cough. The therapy involves educational sessions that teach patients how to control their coughing. This approach is being tested because current drug treatments are not very effective and have significant side effects.
Who is the study for?
This trial is for individuals with any type of Interstitial Lung Disease (ILD) who have been coughing for more than 8 weeks. They must not have had changes in medication, respiratory exacerbations, or upper respiratory infections in the past month and should be able to perform exercise training.
What is being tested?
The study tests a non-drug cough control therapy as an addition to pulmonary rehabilitation for ILD patients with chronic cough. It aims to see if this therapy can reduce the severity and impact of cough without using medications.
What are the potential side effects?
Since the intervention is non-pharmacological, it's expected to have minimal side effects compared to drug treatments. However, specific side effects are not detailed as they may vary depending on individual patient responses.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, average 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, average 1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Feasibility of intervention
Secondary study objectives
Cough Hypersensitivity Questionnaire (CHQ)
Functional Assessment of Chronic Illness Therapy Fatigue Scale (FACIT-F)
Global rating of change questionnaire (GRCQ)
+4 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Non-pharmacological Cough control therapyExperimental Treatment1 Intervention
Participants will attend four virtual sessions of 45 to 60 minutes of educational and self-management. Sessions will be designed to target participants' needs and expectations according to the semi-structured theme.
Session 1 General assessment Prescription of cough technique
Session 2 Cough principles of cough Cough control
Session 3 Breathing pattern retraining and laryngeal hygiene
Session 4 Reinforcement of cough control therapies
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Non-pharmacological treatments for Pulmonary Fibrosis, such as the cough control therapy being studied, primarily involve behavioral and physical techniques aimed at reducing cough severity and its impact on daily life. These methods may include breathing exercises, cough suppression techniques, and pulmonary rehabilitation.
Breathing exercises help improve lung function and oxygenation, while cough suppression techniques teach patients how to control and minimize coughing episodes. Pulmonary rehabilitation combines exercise training, education, and support to enhance overall physical conditioning and respiratory efficiency.
These approaches are crucial for Pulmonary Fibrosis patients as they can alleviate physical discomfort, reduce psychological stress, and improve social interactions, thereby enhancing the quality of life.
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Who is running the clinical trial?
West Park Healthcare CentreLead Sponsor
35 Previous Clinical Trials
2,332 Total Patients Enrolled
1 Trials studying Pulmonary Fibrosis
50 Patients Enrolled for Pulmonary Fibrosis
St. Joseph's Healthcare HamiltonOTHER
201 Previous Clinical Trials
26,929 Total Patients Enrolled
1 Trials studying Pulmonary Fibrosis
60 Patients Enrolled for Pulmonary Fibrosis
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Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Non-pharmacological Cough control therapy
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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