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Resistance Swallowing Training in Patients With Tracheotomy

Fudan University logo

Fudan University

Status

Not yet enrolling

Conditions

Swallowing Training on Muscle Strength

Treatments

Other: progressive resistance swallowing training
Other: pure effortful swallowing

Study type

Interventional

Funder types

Other

Identifiers

NCT06372795
KY2023635

Details and patient eligibility

About

The goal of this clinical trial is to learn investigate the effect of instrument-assisted early progressive resistance swallowing training on swallowing related muscle strength in critically ill patients. It will also learn about the safety of swallowing training. The main questions it aims to answer are:

  • Does instrument-assisted early progressive resistance swallowing training increase the swallowing related muscle strength in critically ill patients?
  • What medical problems do participants have when taking swallowing training?

Researchers will compare instrument-assisted early progressive resistance swallowing training to pure effortful swallowing to see if instrument-assisted early progressive resistance swallowing training works to increase muscle strength.

Participants will:

-Take instrument-assisted early progressive resistance swallowing training or pure effortful swallowing every day for 2 weeks and take muscle strength test every week.

Enrollment

66 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥ 18 years old
  • Tracheotomy after intubation and ventilator ventilation
  • Receiving treatment in ICU, and expected hospital stay > 2 weeks after pneumonectomy
  • Be able to cooperate to complete the maximum anterior tongue pressure test

Exclusion criteria

  • Inability to cooperate with tongue pressure testing and swallowing training, including disturbance of consciousness, oropharyngeal neuromuscular or motor impairment
  • Patients refuse to participate in this study
  • Significant malocclusion and facial asymmetry

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

66 participants in 2 patient groups

Control group
Active Comparator group
Treatment:
Other: pure effortful swallowing
Test group
Experimental group
Treatment:
Other: progressive resistance swallowing training

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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