| Unique ID issued by UMIN | UMIN000061665 |
|---|---|
| Receipt number | R000070555 |
| Scientific Title | A scoping review of populations, intervention characteristics, outcomes, and study designs of breathing technique interventions alone for dyspnea in adult patients with chronic lung disease |
| Date of disclosure of the study information | 2026/05/22 |
| Last modified on | 2026/05/22 19:13:30 |
Breathing technique interventions alone for dyspnea in adult patients with chronic lung disease: a scoping review
Breathing techniques for dyspnea in chronic lung disease
A scoping review of populations, intervention characteristics, outcomes, and study designs of breathing technique interventions alone for dyspnea in adult patients with chronic lung disease
Breathing techniques for dyspnea in chronic lung disease
| Japan |
Chronic lung disease, chronic obstructive pulmonary disease, interstitial lung disease, pulmonary fibrosis
| Pneumology | Nursing | Not applicable |
| Adult |
Others
NO
This scoping review aims to map the existing literature on breathing technique interventions alone for dyspnea in adult patients with chronic lung disease. The review will summarize the populations, target diseases, intervention characteristics, intervention duration, settings, study designs, dyspnea-related outcomes, and reported findings. Eligible breathing techniques include pursed-lip breathing, diaphragmatic breathing, abdominal breathing, deep breathing exercises, breathing control, mindful breathing, and other interventions primarily based on breathing techniques. This review will identify the characteristics of existing studies and evidence gaps to inform future research.
Others
To map the scope, characteristics, outcomes, and evidence gaps of studies on breathing technique interventions alone for dyspnea in patients with chronic lung disease.
The primary outcome of this scoping review will be the specific procedures of breathing technique interventions alone. Extracted information will include the name of the breathing technique, definition of the technique, description of the breathing method, posture during practice, duration per session, frequency, intervention period, instructor, method of instruction, whether the technique was self-administered, relationship with usual care, and information relevant to intervention reproducibility.
The secondary outcomes of this scoping review will be the basic characteristics of included studies, participant and disease characteristics, types and timing of dyspnea-related outcome measures, reported findings, safety, and feasibility. Extracted information will include authors, publication year, country, study design, setting, target disease, age and disease severity of participants, sample size, comparator, dyspnea measurement tools, timing of assessment, dyspnea-related findings, adverse events, adherence, dropout rates, and implementation-related issues.
Others,meta-analysis etc
| 18 | years-old | <= |
| Not applicable |
Male and Female
1. Population
Studies involving adult patients with chronic lung disease will be included.
Eligible diseases include chronic obstructive pulmonary disease (COPD), interstitial lung disease, and pulmonary fibrosis. Participants must be aged 18 years or older.
2. Concept: Intervention
This review will include breathing technique interventions alone that aim to relieve dyspnea.
Eligible interventions include, but are not limited to:
pursed-lip breathing
diaphragmatic breathing
abdominal breathing
deep breathing exercises
breathing control
mindful breathing
other interventions primarily based on breathing techniques
There will be no restrictions on intervention duration. Single-session, short-term, and long-term interventions will all be included.
Studies in which breathing techniques are provided in addition to usual care will also be included.
3. Context
There will be no restrictions on the setting.
Studies conducted in hospitals, outpatient clinics, home settings, rehabilitation facilities, community settings, or other settings will be included.
4. Study Design
Intervention studies will be included.
Eligible study designs include:
randomized controlled trials
crossover trials
quasi-experimental studies
pre-post studies
single-arm intervention studies
5. Outcomes
Studies that include an assessment of dyspnea will be included.
Eligible outcome measures include, but are not limited to:
Borg scale
modified Medical Research Council dyspnea scale (mMRC)
Visual Analog Scale (VAS)
Numerical Rating Scale (NRS)
Baseline Dyspnea Index/Transition Dyspnea Index (BDI/TDI)
University of California, San Diego Shortness of Breath Questionnaire (UCSD SOBQ)
Quality-of-life measures will also be included if they contain dyspnea-related items or subscales.
6. Language and Publication Type
Original articles published in English or Japanese will be included.
1. Ineligible diseases or populations
Studies targeting patients with acute respiratory failure, postoperative patients, patients receiving mechanical ventilation, or healthy participants only will be excluded.
2. Studies targeting diseases other than chronic lung disease
Studies primarily targeting diseases other than chronic lung disease will be excluded. Studies targeting patients with cancer will also be excluded.
3. Studies in which the intervention is not a breathing technique alone
Studies evaluating multicomponent interventions that combine breathing techniques with other components will be excluded. Examples include interventions combined with exercise therapy, muscle strengthening, inspiratory muscle training, yoga as a whole program, tai chi, singing, psychological therapy, educational programs, inhaler instruction, or telerehabilitation.
However, studies in which breathing techniques are provided in addition to usual care will be included.
4. Studies without dyspnea-related outcomes
Studies that do not assess dyspnea-related outcomes will be excluded. For example, studies evaluating only pulmonary function, SpO2, exercise tolerance, or respiratory muscle activity without assessing dyspnea will be excluded.
5. Ineligible study designs or publication types
Reviews, protocols, case reports, case series, qualitative studies, observational studies, cross-sectional studies, commentaries, and conference abstracts without full-text articles will be excluded.
| 1st name | Yohei |
| Middle name | |
| Last name | Kishi |
Mie University
Graduate School of Medicine
5148507
2-174 Edobashi, Tsu
08034330840
326D103@m.mie-u.ac.jp
| 1st name | Yohei |
| Middle name | |
| Last name | Kishi |
Mie University
Graduate School of Medicine
5148507
2-174 Edobashi, Tsu
08034330840
326D103@m.mie-u.ac.jp
Mie University
none
Self funding
N/A
N/A
N/A
N/A
NO
| 2026 | Year | 05 | Month | 22 | Day |
Unpublished
Preinitiation
| 2026 | Year | 05 | Month | 22 | Day |
| 2026 | Year | 05 | Month | 15 | Day |
| 2027 | Year | 05 | Month | 22 | Day |
A comprehensive literature search will be conducted to clarify the definitions and procedures of breathing technique interventions alone for dyspnea in adult patients with chronic lung disease. The electronic databases to be searched will include MEDLINE, CINAHL, the Cochrane Library, and Ichushi-Web. The search will cover articles published from the inception of each database to the date of the search.
Search terms will include "chronic lung disease," "chronic obstructive pulmonary disease," "COPD," "interstitial lung disease," "pulmonary fibrosis," "dyspnea," "breathing technique," "breathing exercise," "pursed-lip breathing," "diaphragmatic breathing," "abdominal breathing," "deep breathing," "breathing control," and "mindful breathing."
Two researchers will independently screen the retrieved records based on the predefined inclusion and exclusion criteria. In the first screening stage, titles and abstracts will be reviewed to assess eligibility. In the second screening stage, the full texts of potentially eligible articles will be reviewed to determine the final inclusion of studies.
If there are discrepancies between the two researchers during the screening process, the decision will be made through discussion. If agreement cannot be reached, a third researcher will be consulted to determine final eligibility.
| 2026 | Year | 05 | Month | 22 | Day |
| 2026 | Year | 05 | Month | 22 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070555