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Efficacy of Inspiratory Muscle Training on Respiratory Performance in Patients With Esophageal Cancer Receiving Combined Modality Therapy

Efficacy of Inspiratory Muscle Training on Respiratory Performance in Patients With Esophageal Cancer Receiving Combined Modality Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03099629
Enrollment
6
Registered
2017-04-04
Start date
2015-03-31
Completion date
2016-10-31
Last updated
2017-04-04

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

Conditions

Esophageal Cancer

Keywords

Inspiratory muscle training, Diaphragmatic surface electromyography, Respiratory muscle strength, Functional capacity

Brief summary

The purpose of this study is to investigate the effectiveness of inspiratory muscle training (IMT) on respiratory performance in patients with esophageal cancer during combined modality therapy.

Detailed description

Background and Purpose: Incidence rates of esophageal cancer remain high in Eastern Asia. In 2012, esophageal cancer was the 9th leading cause of cancer deaths in Taiwan. Whether surgical resection is possible, combined modality therapy is usually required for the treatment of esophageal cancer. In clinical observation, patients underwent combined modality therapy usually demonstrated respiratory muscle dysfunction which might further impair physical activity and quality of life. The purpose of this study is to investigate the effectiveness of inspiratory muscle training (IMT) on respiratory performance in patients with esophageal cancer during combined modality therapy. Methods: This is a prospective interventional study design. A total of 45 patients with newly diagnosed esophageal cancer will be recruited from the Mackay Memorial Hospital. All tests will be performed at baseline (prior to cancer treatment), weekly during treatment, prior to surgery, and one month after surgery. Tests will include demographic data collection, respiratory muscle performance (maximal inspiratory and expiratory pressure tests combined with diaphragmatic surface electromyography, and pulmonary functional test), dyspnea, and the functional exercise test (6-min walk test). IMT will start with an intensity of 30% of maximal inspiratory pressure, 15 times/set, 3 sets/day, 7 days/week and training will continue until surgery is scheduled or 2 weeks after the completion of treatment if surgery is not suitable. Repeated measure ANOVA will be used for analyzing difference of parameters among various time points. Clinical relevance: The results of this study will help to better understand the clinical beneficial effects (e.g., better functional capacity) of an added inspiratory muscle training during combined modality therapy in patients with esophageal cancer.

Interventions

BEHAVIORALinspiratory muscle training

inspiratory muscle training will start with an intensity of 30% of maximal inspiratory pressure, 15 times/set, 3 sets/day, 7 days/week and training will continue until surgery is scheduled or 2 weeks after the completion of treatment if surgery is not suitable.

Sponsors

Mackay Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* newly diagnosed primary esophageal cancer, aged more than 20 years, communicate without difficulty.

Exclusion criteria

* inability to perform inspiratory muscle training, the presence of unstable angina or myocardial infarction in recently one month, cannot cooperate with training protocols, and pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Changes of maximal expiratory pressure (MEP)Baseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline MEP at the end of each week's CCRT treatment
Changes of forced expiratory volume in one second (FEV1)Baseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline FEV1 at the end of each week's CCRT treatment
Changes of forced vital capacity (FVC)Baseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline FVC at the end of each week's CCRT treatment
Changes of maximal inspiratory pressure (MIP)Baseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline MIP at the end of each week's CCRT treatment
Changes of diaphragmatic surface electromyography (EMGdi)Baseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline EMGdi at the end of each week's CCRT treatment

Secondary

MeasureTime frameDescription
Changes of dyspnea using Modified Borg Dyspnea scoreBaseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline Modified Borg Dyspnea score at the end of each week's CCRT treatment
Changes of functional exercise capacity using 6-minute walking distanceBaseline and weekly during CCRT treatment (for a total of 4-5 weeks)Change from baseline 6-minute walking distance at the end of each week's CCRT treatment

Countries

Taiwan

Outcome results

None listed

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