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Effect of intelligent inspiratory muscle training on patients with esophageal cancer following esophagectomy: a randomized controlled trial

Effect of intelligent inspiratory muscle training on patients with esophageal cancer following esophagectomy: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077140
Enrollment
Unknown
Registered
2023-10-31
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

Esophageal cancer

Interventions

Experimental group:The intervention group will receive an intelligent inspiratory muscle training program using a portable device.
Control group:The control group will receive a regular inspiratory muscle training program, which is currently part of usual care.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria are as follows: (1) esophageal cancer patients aged 18 years or more; (2) scheduled for esophagectomy by either a transhiatal esophageal resection (THE), a transthoracic esophageal resection (TTE), or minimally invasive (robot-assisted or conventional) thoracolaparoscopic esophageal resection (MIE); (3) capable of performing inspiratory muscle training; (4) willing to participant in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: (1) receive a respiratory training or rehabilitation training program within 8 weeks; (2) receive a thoracotomy before; (3) chronic obstructive pulmonary disease; (4) other types of cancer; (5) with a history of mental disease; (6) cognitive dysfunction assessed by Mini-mental State Examination (MMSE) (a MMSE score of 17 or less for illiterate participants, 20 for primary school, and 24 for junior high school and above; (7) cardiac function graded as IV according to New York Heart Association (NYHA); (8) uncontrolled blood pressure (systolic/diastolic blood pressure =140/90 mmHg); (9) preoperative mechanical circulatory support, such as intra-aortic balloon counterpulsation (IABC), or extracorporeal membrane oxygenation (ECMO), or preoperative intubation.

Design outcomes

Primary

MeasureTime frame
The incidence of postoperative pulmonary complication within the first 7 postoperative days;Pulmonary function;Physical function;Patient-reported outcome;Training adherence;

Secondary

MeasureTime frame
Adverse events;Length of hospital stay;Life-space mobility;Hospital cost;The participants’ willingness to undergo inspiratory muscle training;

Countries

China

Contacts

Public ContactLin Lin

West China Hospital, Sichuan University

94592651@qq.com+86 189 8060 6317

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026