Effectiveness of interdisciplinary swallowing care on prevention of aspiration pneumonia, using ultrasound-based observation of swallowing function in community dwelling adults

Effectiveness of interdisciplinary swallowing care on prevention of aspiration pneumonia, using ultrasound-based observation of swallowing function in community dwelling adults - Effectiveness of ultrasound-based swallowing care on prevention of aspiration pneumonia in community dwelling adults

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000035140

Enrollment

Registered

2018-12-05

Start date

2018-02-19

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

dysphagia

Interventions

Baseline phase: participants receive the standard swallowing care based on the conventional observation and tests for 4-6 weeks. Intervention phase: participants receive the interdisciplinary swallow

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Person performing oral intake at sitting or reclining position Person who had experienced choking within the last 6 month

Exclusion criteria

Exclusion criteria: presence of a tracheotomy hole presence of a systemic infection presence of a sever cognitive impairment presence of a psychiatric disease Person whose physicians have determined that they are not eligible for the study

Design outcomes

Primary

Measure	Time frame
incidence of aspiration pneumonia during research period (16-18 weeks)	—

Secondary

Measure	Time frame
safe oral intake level	—

Countries

Japan

Contacts

Public ContactMikako Yoshida

The University of Tokyo, Graduate School of Medicine Department of Imaging Nursing Science

mokka-tky@umin.ac.jp0358413451

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026