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Not yet recruiting NCT07550335

Group Reading and Oral Exercise Program for Older Adults

No phase Interventional Oral Frailty Depression Sarcopenia Physical Function Decline

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Reading and Oral Exercise Program.
Who it may be relevant to
Registry conditions: Oral Frailty, Depression, Sarcopenia, Physical Function Decline. Basic parameters: from 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects of a Focus Group-Based Bibliotherapy Intervention Combined With Oral Exercises on Oral Frailty, Physical Function, Grit, and Depression in Community-Dwelling Older Adults

Overview

Depression is common among older adults and is often associated with declines in physical and oral health. Non-pharmacological, community-based interventions are needed to support both mental and physical well-being. This study examines the effects of a program combining group-based reading activities and oral exercises in community-dwelling older adults. Participants are randomly assigned to either an intervention group, which receives the six-week program, or a control group receiving general oral health education. The study evaluates whether the intervention can improve physical and oral function, enhance psychological resilience (grit), and reduce depressive symptoms.

Interventions

  • Behavioral Reading and Oral Exercise Program
    Participants in the intervention group receive a combined program of group-based reading activities and oral exercises. The program is delivered in a focus group format and includes guided reading discussions to promote emotional expression and reflection, along with structured oral exercises to enhance oral muscle function. The intervention is conducted over a 6-week period, with sessions held once every two weeks for a total of three sessions.

Primary outcome measures

  • Depressive Symptoms [Time frame: At baseline and immediately after the 6-week intervention period]
Secondary outcome measures (3)
  • Oral Frailty [Time frame: At baseline and immediately after the 6-week intervention period]
  • Sarcopenia Risk [Time frame: At baseline and immediately after the 6-week intervention period]
  • Grit [Time frame: At baseline and immediately after the 6-week intervention period]

Eligibility criteria

Inclusion criteria

  • Community-dwelling adults aged 55 years and older.
  • Able to communicate in Mandarin or Taiwanese and capable of understanding study instructions and participating in group discussions.
  • Able to complete study questionnaires independently or with assistance from research staff.

Exclusion criteria

  • Individuals with severe cognitive impairment that precludes understanding study procedures or participation in group discussions.
  • Individuals with a current diagnosis of severe psychiatric disorders (e.g., schizophrenia, acute phase of bipolar disorder) that would make participation in group activities inappropriate.
  • Individuals who have participated in similar psychological or bibliotherapy-based interventions within the past 3 months.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07550335 · 26MMHIS046e

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗