跳至主要内容
临床试验/NCT07550335
NCT07550335尚未招募不适用

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

Mackay Memorial Hospital0 个研究点目标入组 60 人开始时间: 2026年4月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Depressive Symptoms

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
55 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

Intervention Group

Experimental

干预措施: Reading and Oral Exercise Program (Behavioral)

Control Group

No Intervention

结局指标

主要结局

Depressive Symptoms

时间窗: At baseline and immediately after the 6-week intervention period

Depressive symptoms measured using the Geriatric Depression Scale (GDS), with higher scores indicating more severe depressive symptoms.

次要结局

  • Oral Frailty(At baseline and immediately after the 6-week intervention period)
  • Sarcopenia Risk(At baseline and immediately after the 6-week intervention period)
  • Grit(At baseline and immediately after the 6-week intervention period)

研究者

申办方类型
Other
责任方
Sponsor

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