# Inspiratory muscle training and aerobic exercise for respiratory muscle strength in myasthenia gravis post-hospitalization- a randomized controlled trial

**Authors:** Chia-Ling Chang, Tien-Pei Fang, Hsin-Mao Tsai, Hui-Chin Chen, Shih-Feng Liu, Hui-Ling Lin, Jui-Fang Liu

PMC · DOI: 10.1186/s12890-025-03733-7 · BMC Pulmonary Medicine · 2025-05-27

## TL;DR

A six-week program combining breathing exercises and aerobic activity improved lung strength and physical capacity in myasthenia gravis patients after hospital discharge.

## Contribution

This is the first randomized controlled trial to evaluate the combined effects of inspiratory muscle training and aerobic exercise in post-hospitalized myasthenia gravis patients.

## Key findings

- The IMT + AE group showed significant improvements in forced vital capacity and respiratory muscle strength.
- Participants in the IMT + AE group experienced reduced dyspnea and increased walking distance compared to controls.
- The control group showed decreased lung volumes, while the IMT + AE group showed improvements.

## Abstract

Previous studies have demonstrated the positive effects of long-term inspiratory muscle training (IMT) on inspiratory muscle strength and pulmonary function. However, the benefits of IMT with aerobic exercise (IMT + AE) in patients with myasthenia gravis (MG) remain unclear. This randomized controlled trial aimed to assess the impact of the early, 6-week, moderate-intensity interval IMT + AE on pulmonary function, functional capacity, and respiratory muscle strength in patients with MG post-hospitalization.

Patients with Discharged MG were randomly assigned to either a control group receiving standard medical management or an intervention group undergoing six-week IMT + AE program. Respiratory status was evaluated using the maximum inspiratory/expiratory pressure (MIP/MEP) and pulmonary function tests. Modified Borg dyspnea scores and a six-minute walk test for functional capacity were also employed.

Fifty-four participants were assigned to either the control (sixn = 28) or IMT + AE groups (n = 26). At 6 weeks, the IMT + AE group showed significant improvements across all parameters, while the control group only showed notable differences in the modified Borg scale scores and walking distance. MIP improvements were 33.8 ± 36.1 cmH2O in IMT and 22.1 ± 25.8 cmH2O in control groups (P = 0.18). The IMT + AE group improvements were more substantial in MEP, modified Borg scale, and 6-minute walk distance, in addition to forced vital capacity (FVC) and FVC % of prediction (0.21 ± 0.24 L and 6.17 ± 6.01%, respectively), while the control group showed decreased volumes (-0.06 ± 0.30 L and − 1.79 ± 9.69%, respectively). FVC improvement was significant with IMT + AE (0.21 ± 0.24 L) vs. reduction in the control group (-0.06 ± 0.3 L; P = 0.001).

Implementing six-week moderate-intensity interval IMT + AE effectively enhanced respiratory muscle strength, alleviated dyspnea, improved physical capacity, and increased FVC in patients with MG following hospitalization after discharge.

The study was registered in The Clinical Trials Clinical Trial (NCT06624345||https://www.clinicaltrials.gov/) on October 12, 2024 (retrospectively registered).

The online version contains supplementary material available at 10.1186/s12890-025-03733-7.

## Linked entities

- **Diseases:** myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Diseases:** myasthenia gravis (MESH:D009157), dyspnea (MESH:D004417)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12107784/full.md

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Source: https://tomesphere.com/paper/PMC12107784