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Completed

NCT Number: NCT06617143

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

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.

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Key information

Conditions

Asthma Anxiety Disorders Behavior Behavioral Symptoms Bronchial Diseases Depression Dyspnea Hypersensitivity Hypersensitivity, Immediate Immune System Diseases Lung Diseases Lung Diseases, Obstructive Mental Disorders Mindfulness Pathological Conditions, Signs and Symptoms Respiration Disorders Respiratory Hypersensitivity Respiratory Tract Diseases Signs and Symptoms Signs and Symptoms, Respiratory

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ardahan University

Ardahan, 75100, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Mindfulness-based cognitive therapy

Other

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

Other

routine treatment and care

Primary outcomes

  1. Anxiety

    Time frame: Average of 1 week after completion of the intervention

    It will be evaluated with the Hospital Anxiety and Depression Scale.

  2. Depression

    Time frame: Average of 1 week after completion of the intervention

    It will be evaluated with the Hospital Anxiety and Depression Scale.

  3. Dyspnea

    Time frame: Average of 1 week after completion of the intervention

    It will be assessed with the Modified Medical Research Council (mMRC) Dyspnoea Questionnaire.

Sponsors and collaborators

Lead sponsor

Ardahan University

Other

Registry information

Official study title

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

Acronym: MBCT

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Sep 27, 2024
Registry last updated
Aug 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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