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Effect of MBCT Applied to Asthma Patients on Anxiety, Depressıon and Dyspnea

Effects of Short-Term Conscious Awareness-Based Cognitıve Therapy Applied to Asthma Patients on Anxiety, Depression and Dyspnea

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06617143
Acronym
MBCT
Enrollment
48
Registered
2024-09-27
Start date
2025-04-01
Completion date
2025-08-15
Last updated
2025-08-27

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

Conditions

Asthma, Mindfulness

Keywords

asthma, mindfulness-based cognitive therapy, anxiety, depression, dyspnea

Brief summary

In this study, short-term MBCT will be applied to asthmatic patients receiving hospital treatment and its effects on anxiety, depression and dyspnea will be determined. A quasi-experimental study was planned for this purpose.

Detailed description

In the study, cognitive behavioral therapy will be applied to the intervention group, which is determined as the experimental group, and a group of asthma patients who did not receive any application during the same periods will be included and the dyspnea, anxiety and depression levels of the patients in these two groups will be compared.

Interventions

OTHERmindfulness-based cognitive therapy

In this study, it is planned to apply MBCT to asthmatic inpatients in the patient room in groups of 2 or 3. This application is planned to continue for one hour.

routine treatment and care

Sponsors

Ardahan University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

Participants and researchers could not be blinded due to the natural course of the study and only the statistician was blinded.

Intervention model description

pre-test post-test quasi-experimental design

Eligibility

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

Inclusion criteria

Over 18 years old, Inpatient treatment in the chest ward volunteer participants with no communication problems

Exclusion criteria

Under 18 years old, with communication problems, not willing to participate hospitalized with diseases other than asthma

Design outcomes

Primary

MeasureTime frameDescription
AnxietyAverage of 1 week after completion of the interventionIt will be evaluated with the Hospital Anxiety and Depression Scale.
DepressionAverage of 1 week after completion of the interventionIt will be evaluated with the Hospital Anxiety and Depression Scale.
DyspneaAverage of 1 week after completion of the interventionIt will be assessed with the Modified Medical Research Council (mMRC) Dyspnoea Questionnaire.

Countries

Turkey (Türkiye)

Outcome results

None listed

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