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NCT Number: NCT07626749

DDK Acoustic Analysis and Swallowing Indicators

This study examines whether simple speech tasks and a swallowing screening test can help identify swallowing risk in adults of different ages. Participants will complete basic questions, a swallowing self-assessment, a saliva swallowing test, and short voice recordings of rapid syllables. The study is non-invasive, takes about 75 minutes, and may help develop an easy, low-cost screening tool for early swallowing problems.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Sports Medicine, Kaohsiung Medical University, Taiwan

Kaohsiung City, Taiwan, 807

Location contact

C F HUNG, MASTER

CONTACT

[email protected]

+8867-3121101 ext. #2646 #624

C F HUNG, Master

SUB_INVESTIGATOR

L Y GUO Professor and Dean of the college of Health Sciences, Doctorate

CONTACT

[email protected]

+8867-3121101 ext. #2646 #624

About this study

This is a cross-sectional observational study examining the relationship between diadochokinetic (DDK) speech performance and swallowing function in community-dwelling adults aged 18 years and older. Participants will complete a single study visit, during which demographic and health-related information will be collected, the EAT-10 swallowing self-assessment will be administered, the Repetitive Saliva Swallowing Test (RSST) will be performed, and short DDK speech recordings of /pa/, /ta/, and /ka/ will be obtained in a quiet setting. Acoustic features will be extracted from the recordings and analyzed together with RSST and EAT-10 results to explore age-related differences and to develop a predictive screening model for swallowing risk. All data will be de-identified, securely stored, and retained according to study requirements.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1.Community-dwelling adults aged 18 years or older, with no upper age limit.
  • 2.Ability to communicate in Mandarin or Taiwanese and understand the study procedures.
  • 3.Willingness to provide written informed consent.
  • 4 .Ability to complete the DDK tasks and RSST.

Exclusion criteria

  • 1.Presence of acute respiratory infection, upper respiratory inflammation, or other acute conditions that may significantly affect speech or swallowing.
  • 2.Impaired consciousness, significant cognitive deficits, or inability to understand the study procedures.
  • 3.Recent surgery or radiotherapy involving the oral cavity or pharynx that affects speech or swallowing.
  • 4.Severe hearing impairment that prevents understanding of instructions.
  • 5.Any other condition deemed unsuitable for participation by the investigators.

Treatment and study plan

Primary outcomes

  1. Repetitive Saliva Swallowing Test Classification

    Time frame: Day 1

    Classification of swallowing function based on the Repetitive Saliva Swallowing Test (RSST). Participants will be classified as having normal RSST performance if they complete greater than or equal to 3 swallows in 30 seconds, and abnormal RSST performance if they complete fewer than 3 swallows in 30 seconds.

Secondary outcomes

  1. Eating Assessment Tool-10 Total Score

    Time frame: Day 1

    Total score on the Eating Assessment Tool-10 (EAT-10), a 10-item self-report questionnaire used to assess swallowing-related symptoms. The total score ranges from 0 to 40, where higher scores indicate worse swallowing-related symptoms. A score of 3 or higher suggests possible swallowing difficulty.

  2. Diadochokinetic Speech Rate

    Time frame: Day 1

    Rate of repeated diadochokinetic speech productions of /pa/, /ta/, and /ka/. The rate will be reported as syllables per second.

  3. Diadochokinetic Speech Fundamental Frequency

    Time frame: Day 1

    Fundamental frequency (F0) extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. Fundamental frequency will be reported in Hertz (Hz).

  4. Diadochokinetic Speech First Formant Frequency

    Time frame: Day 1

    First formant frequency (F1) extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. F1 reflects the first resonance frequency of the vocal tract and will be reported in Hertz (Hz).

  5. Diadochokinetic Speech Second Formant Frequency

    Time frame: Day 1

    Second formant frequency (F2) extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. F2 reflects the second resonance frequency of the vocal tract and will be reported in Hertz (Hz).

  6. Diadochokinetic Speech Jitter

    Time frame: Day 1

    Jitter extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. Jitter reflects short-term cycle-to-cycle variability in fundamental frequency and will be reported as a percentage.

  7. Diadochokinetic Speech Shimmer

    Time frame: Day 1

    Shimmer extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. Shimmer reflects short-term variability in voice amplitude and will be reported in decibels (dB).

  8. Diadochokinetic Speech Harmonics-to-Noise Ratio

    Time frame: Day 1

    Harmonics-to-noise ratio (HNR) extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. HNR reflects the ratio of periodic harmonic energy to noise energy in the voice signal and will be reported in decibels (dB).

  9. Diadochokinetic Speech Root Mean Square Amplitude

    Time frame: Day 1

    Root mean square (RMS) amplitude extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. RMS amplitude reflects the average acoustic energy of the speech signal and will be reported in normalized amplitude units.

  10. Diadochokinetic Speech Zero-Crossing Rate

    Time frame: Day 1

    Zero-crossing rate (ZCR) extracted from repeated diadochokinetic (DDK) speech recordings of /pa/, /ta/, and /ka/. ZCR reflects the rate at which the speech signal changes sign over time and will be reported as the number of zero crossings per second.

Other outcomes

  1. Participant Age

    Time frame: Day 1

    Age of participants collected at baseline, reported in years.

  2. Participant Sex

    Time frame: Day 1

    Sex of participants collected on Day 1, reported as male or female according to the study case report form.

  3. Education Level

    Time frame: Day 1

    Highest level of education completed by participants collected at baseline, categorized as primary school or below, junior high school, senior high school, or college or above.

  4. Body Mass Index

    Time frame: Day 1

    Body mass index (BMI) calculated from measured height and weight at baseline. Height will be measured in meters and weight in kilograms; BMI will be reported in kg/m².

  5. Dentition Status

    Time frame: Day 1

    Dentition status of participants collected at day 1, categorized as natural dentition, partial denture, full denture, or other.

  6. Dry Mouth Frequency

    Time frame: Day 1

    Self-reported frequency of dry mouth symptoms collected at day 1, categorized as never, occasionally, frequently, or always.

  7. Smoking History

    Time frame: Day 1

    Self-reported smoking history collected at baseline, categorized as never smoker, former smoker, or current smoker.

  8. Medical History

    Time frame: Day 1

    Self-reported medical history collected at day 1 and categorized as none, hypertension, hyperglycemia, hyperlipidemia, or gastrointestinal disease (such as gastroesophageal reflux disease).

Study contacts

Contact information is provided by the study sponsor or research team.

HUNG C F Kaohsiung Medical University, MASTER

CONTACT

[email protected]

+8867-3121101 ext. #2646 #614

Sponsors and collaborators

Lead sponsor

Kaohsiung Medical University

Other

Registry information

Official study title

Acoustic Analysis of Performance in Diadochokinetic (DDK) Tasks and Swallowing Function Indicators Among Adults Across Different Age Groups

Acronym: AAP-DDK

Important dates

Study start
2026
Primary completion
2030
Study completion
2030
First posted
Jun 4, 2026
Registry last updated
Jun 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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