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Updated: Jan 11, 2026

Adapting Human Videofluoroscopic Swallow Study Methods to Detect and Characterize Dysphagia in Murine Disease Models
Published on: March 1, 2015
Swallowing behavior response to semi-solid foods with different textural properties in healthy older adults: an
Masashi Tsujimoto1, Tomoko Hisajima2, Saho Matsuda3
1National Center for Geriatrics and Gerontology, Innovation Center for Translational Research, 7-430 Morioka-cho, Obu, Aichi, Japan.
Background:
Semi-solid foods are widely consumed by older adults, yet the influence of their physical properties on swallowing remains unclear.
Objectives:
To examine how variations in shape retention and spreadability affect swallowing in adults aged ≥75 years.
Design:
An open-label randomized crossover trial with two food tests.
Setting:
Controlled experimental setting.
Participants And Numbers Analyzed:
Test 1 enrolled 21 adults and Test 2 enrolled 28; after exclusions, 14 and 16 were analyzed (mean ages 81.6 and 78.6 years).
Interventions:
Participants ingested three semi-solid foods (P, Q, S) differing in physical properties.
Outcomes:
Primary outcomes were oral processing time (OPT) and swallowing duration (SD), measured by a neck-worn electronic stethoscope and synchronized video. Secondary outcomes were subjective ratings of swallowing ease and food properties. Medians of five bites were analyzed, and first-fifth bite differences assessed.
Results:
Subjective ratings differed only in collectability in Test 2. In Test 1, OPT was longer for P than Q (median difference 1.04 s, 95 % CI 0.15-2.04; p = 0.030). In Test 2, OPT was longer for S than P (median difference -1.88 s, -2.81 to -0.74; p = 0.001). SD did not differ significantly. With repeated swallows, OPT variance increased and SD variance decreased for P and Q, while both increased for S.
Harms:
None observed.
Conclusions:
Semi-solid food properties affect swallowing in older adults. Shape retention contributes to distinct swallowing patterns, supporting individualized food selection to promote safe intake.
Trial Registration:
UMIN000053442, UMIN000056840.
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