Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07021586

Tongue Pressure in Middle-Aged and Elderly Individuals With Chronic Cervical Pain

Status
Recruiting
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
National Yang Ming Chiao Tung University · Academic / Other
Sex
All
Age
50 Years – 65 Years
Healthy volunteers
Accepted

Summary

The goal of the cross-sectional study is to explore the impact of neck pain on tongue pressure in the middle-aged and elderly population and analyze the effects of different cranio-cervical positioning on tongue pressure performance. The main questions it aims to answer are: 1. Do middle-aged and elderly individuals with chronic cervical pain exhibit reduced maximal tongue pressure compared to those without cervical pain? 2. What are the effects of different cranio-cervical positioning on tongue pressure performance? Participants will complete all the assessments on the day of testing.

Detailed description

1\. For Quality assurance plan that addresses data validation and registry procedures: (1) Relevant data will be recorded by the researchers. All assessments will be conducted in the Orthopedic Laboratory at National Yang Ming Chiao Tung University, where the equipment is regularly maintained and monitored. 2\. For Standard operating procedures to address registry operations and analysis activities: (1 ) Participants will be recruited from clinics and communities in the Taipei and New Taipei City. Collected data will include personal information such as height, age, weight, and the number of removable dentures. Data management and analysis will be conducted using laboratory-designated computers for data storage and processing. Any adverse events, such as throat or tongue soreness occurring within 1-2 days after testing, will be recorded and reported to the researchers. 3\. For Sample size assessment: (1) Total forty participants aged between 50-65 years. 4\. For missing data: (1) This study is a cross-sectional, single-session assessment, and therefore the likelihood of missing data is minimal and no specific handling procedures are needed. 5\. For statistical analysis: (1) Data analysis for this study was conducted using SPSS software version 29.0. Continuous and categorical variables were compared between the two groups using independent t-tests and chi-square tests. Other outcomes will be analyzed using two-way mixed ANOVA, independent t-tests, or Pearson's correlation coefficient to compare differences between groups or examine associations. The significance level is set at 0.05, with p-values less than 0.05 considered statistically significant.

Conditions

Timeline

Start date
2025-02-20
Primary completion
2025-06-30
Completion
2025-06-30
First posted
2025-06-15
Last updated
2025-06-15

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT07021586. Inclusion in this directory is not an endorsement.