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Enrolling By InvitationNCT07265726

Oral Health Education for Older Adults: Intentionality in Action

Exploring the Effectiveness of the Intentionality the Matrix of Healing in Enhancing Oral Health Education Outcomes for Community-dwelling Middle-aged and Older

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Mackay Memorial Hospital · Academic / Other
Sex
All
Age
40 Years – 100 Years
Healthy volunteers
Accepted

Summary

After obtaining approval from the Institutional Review Board (IRB), the clinical trial will be registered on a designated trial registration website. Participant recruitment will be conducted online. For individuals who meet the inclusion criteria and express interest, the principal investigator will verbally explain the study protocol, go over the informed consent form, and answer any related questions. Potential participants who meet the inclusion criteria and are willing to participate will be given time to consider their involvement in the study. Inclusion criteria for this study are: 1. Adults aged 40 and older 2. Ability to hear, speak, and read Chinese, and communicate fluently in Mandarin or Taiwanese. Exclusion criteria include: 1. Being completely edentulous and not using dentures; 2. Having severe food allergies, renal failure, or dysphagia; 3. Being diagnosed with terminal illness under palliative care, severe mental illness, or cognitive impairment; 4. Having a serious health condition that prevents standing or performing oral self-care behaviors. Upon receiving verbal agreement from potential participants, the study procedure and the contents of the consent form will be explained again. This is a parallel randomized experimental study, with an estimated sample of 90 middle-aged and older adults recruited from the community through online means. Participants will be randomly assigned to one of three groups: 1. intentional interviews combined with expressive arts activities, 2. expressive arts activities only, or 3. control group. All three groups will receive oral health education before the intervention and six weeks after the intervention. Questionnaire surveys will be conducted one week and one month post-education to collect data on sarcopenia risk, eating assessment, grit, oral health literacy, and oral self-care behaviors. Statistical analyses will be performed on the collected data. Participants who fully understand the study and agree to participate will sign an informed consent form. Two copies of the consent form will be prepared-one will be kept by the principal investigator, and a photocopy will be given to the participant for personal recordkeeping. Participants retain the right to decline or withdraw from the study at any time, even after signing the consent form. Their withdrawal will not affect their future rights, benefits, or services, and any previously collected data will be deleted upon request.

Conditions

Interventions

TypeNameDescription
BEHAVIORALIntentional InterviewParticipants in this arm will receive an intervention
BEHAVIORALExpressive Arts ActivitiesParticipants in this arm will engage only in expressive arts activities over a 6-week period.

Timeline

Start date
2025-07-02
Primary completion
2026-07-31
Completion
2026-07-31
First posted
2025-12-05
Last updated
2025-12-05

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT07265726. Inclusion in this directory is not an endorsement.