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Group Reading and Oral Exercise Program for Older Adults

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07550335
Enrollment
60
Registered
2026-04-24
Start date
2026-04-23
Completion date
2027-12-31
Last updated
2026-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Oral Frailty, Physical Function Decline, Sarcopenia

Brief summary

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

BEHAVIORALReading 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.

Sponsors

Mackay Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Community-dwelling adults aged 55 years and older. 2. Able to communicate in Mandarin or Taiwanese and capable of understanding study instructions and participating in group discussions. 3. Able to complete study questionnaires independently or with assistance from research staff.

Exclusion criteria

1. Individuals with severe cognitive impairment that precludes understanding study procedures or participation in group discussions. 2. 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. 3. Individuals who have participated in similar psychological or bibliotherapy-based interventions within the past 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Depressive SymptomsAt baseline and immediately after the 6-week intervention periodDepressive symptoms measured using the Geriatric Depression Scale (GDS), with higher scores indicating more severe depressive symptoms.

Secondary

MeasureTime frameDescription
Oral FrailtyAt baseline and immediately after the 6-week intervention periodOral frailty assessed using the Oral Frailty Index, with higher scores indicating greater oral frailty.
Sarcopenia RiskAt baseline and immediately after the 6-week intervention periodSarcopenia risk assessed using the SARC-F questionnaire, with higher scores indicating greater risk of sarcopenia
GritAt baseline and immediately after the 6-week intervention periodGrit assessed using the Grit Scale, with higher scores indicating greater perseverance and consistency of interest.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026