# Establishing the minimal clinically important difference of the 6-min walk test in lung transplant recipients undergoing pulmonary rehabilitation: a prospective analysis

**Authors:** Peijian Wang, Beiyao Gao, Jing Sun, Yang Yu, Lijun Ge, Shan Jiang, Siyuan Wang, Wenhui Chen

PMC · DOI: 10.3389/fmed.2026.1740439 · Frontiers in Medicine · 2026-01-21

## TL;DR

This study determines the minimal clinically important difference for the 6-minute walk test in lung transplant recipients after pulmonary rehabilitation.

## Contribution

The study establishes a specific MCID value for the 6MWT in lung transplant recipients undergoing PR.

## Key findings

- The 6MWT distance improved significantly by 73.37 meters after pulmonary rehabilitation.
- Changes in handgrip strength were strongly correlated with changes in 6MWT distance.
- The MCID for the 6MWT was estimated at 56.83 meters using combined methods.

## Abstract

This study aimed to evaluate the responsiveness of the 6-min walk test (6MWT) to pulmonary rehabilitation (PR) in lung transplant recipients (LTRs) and to establish the minimum clinically important difference (MCID) for the 6MWT in this population.

Eighty-one LTRs from a single-center randomized controlled trial were included. The MCID was calculated using anchor-based (handgrip strength) and distribution-based methods. Handgrip strength (left, right, and average) and 6MWT distance were assessed before and after an 8-week PR program.

All 81 participants completed PR. The 6MWT distance improved significantly, with a mean change of 73.37 m (Cohen’s d = 1.10). Handgrip strength increased by 7.24–8.21 kg (Cohen’s d = 0.80–0.91; all p < 0.001). Changes in handgrip strength were strongly correlated with changes in 6MWT distance (r = 0.63–0.69; p < 0.001). The MCID was estimated at 52.65–58.5 m (anchor-based), 57.28–59.40 m (distribution-based), and 56.83 m (combined).

The 6MWT is responsive to PR in LTRs. A MCID of 56.83 m provides a clinically meaningful benchmark for interpreting exercise capacity changes and can guide sample size estimation in future trials.

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** cardiac, cerebral, hepatic, or renal dysfunction (MESH:D006331), end-stage lung diseases (MESH:D058625), IPF (MESH:D054990), ILD (MESH:D017563), metabolic acidosis (MESH:D000138), infection (MESH:D007239), EID (MESH:D000092202), dyspnea (MESH:D004417), LTRs (MESH:D008171), COPD (MESH:D029424), muscle weakness (MESH:D018908), psychiatric, cognitive, or musculoskeletal disorders (MESH:D001523), BOS (MESH:C537415), skeletal muscle dysfunction (MESH:D009135), pulmonary fibrosis (MESH:D011658), bronchiolitis obliterans syndrome (MESH:D000092122), pulmonary hypertension (MESH:D006976), MCID (MESH:D000076263), fatigue (MESH:D005221), respiratory disease (MESH:D012140)
- **Chemicals:** oxygen (MESH:D010100), PR (-)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868253/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868253/full.md

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Source: https://tomesphere.com/paper/PMC12868253