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Group Telehealth Behavioral Cough Suppression Therapy

Group Telehealth Behavioral Cough Suppression Therapy Pilot Study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06706765
Enrollment
60
Registered
2024-11-27
Start date
2024-03-22
Completion date
2025-01-31
Last updated
2024-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Refractory Chronic Cough

Brief summary

The purpose of this study is to investigate the effectiveness of behavioral cough suppression therapy (BCST) in managing refractory chronic cough (RCC) within a group telehealth setting. RCC is a cough that has lasted at least 8 weeks and has not resolved with standard medical treatment. BCST is a research-based treatment provided by specialty-trained speech-language pathologists (SLPs) for patients with RCC. Although the treatment works very well for a large proportion of patients in a standard one-on-one format, there are a limited number of SLPs available to provide this treatment and patients living in rural areas do not typically have access to an SLP trained in BCST. If BCST can effectively be delivered in a group telehealth model, it would significantly improve accessibility to the treatment.

Interventions

BEHAVIORALBehavioral Treatment

Behavioral cough suppression therapy delivered in a group setting via telehealth.

Sponsors

University of Montana
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* At least 18 years old * Predominantly dry cough for at least 8 weeks * Evaluated and treated by at least one physician for cough * Obtained a chest X-ray or chest CT scan specifically related to the cough with unremarkable results * Access to a computer or tablet that includes a camera and able to use the device independently * Reliable internet access * Willing to agree to maintain confidentiality of personal information (including names) related to others in the study

Exclusion criteria

* Under age 18 * Coughing up blood * Current smoker of any substance * History of smoking or 10 or more years * Diagnosed with a chronic lung condition (e.g., COPD, emphysema, lung cancer, idiopathic pulmonary fibrosis, chronic bronchitis, asthma)? (NOTE: If a patient has been told their cough may be (or is likely) due to asthma but they have not had any formal lung testing and asthma treatments have not helped your cough, we don't consider this a formal asthma diagnosis and will not exclude them from the study.) * Diagnosed currently or in the past with head and neck cancer (i.e., cancer of the mouth, nose, or throat). * Complaints of swallowing difficulty * Taking any of the following medications, which have a known side effect of cough: Benzapril (Lotensin), Captopril (Capoten), Enalapril/Enalaprilat (Vasotec oral and injectable), Fosinopril (Monopril), Lisinopril (Zestril and Prinivil), Moexipril (Univasc), Perindopril (Aceon), Quinapril (Accupril), Ramipril (Altace), and Trandolapril (Mavik) * Prior BCST treatment with an SLP or respiratory therapist

Design outcomes

Primary

MeasureTime frameDescription
Leicester Cough QuestionnaireBaseline, one-week post-treatment, and one-month post-treatmentThe Leicester Cough Questionnaire is a 19-item self-report questionnaire that is valid and reliable, and repeatable every two weeks. The total possible score is 21. The higher the score the better the cough-related quality of life.

Secondary

MeasureTime frameDescription
Patient Global Impression of Severity Scale in Chronic CoughBaseline, every treatment session (4-6 treatment sessions, one treatment session per week), and one-month post-treatmentThe Patient Global Impression of Severity Scale in Chronic Cough involves the patient answering the question how do you rate your overall current cough severity? with options of no problem, mild, moderate, or severe problem.

Countries

United States

Contacts

Primary ContactJane E Reynolds, PhD
jane.reynolds@mso.umt.edu406-243-2138
Backup ContactLaurie J Slovarp, PhD
laurie.slovarp@mso.umt.edu406-243-2107

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026