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Evaluating a wellbeing clinic to support older adults with mild to moderate dementia living in residential aged care settings

Not Applicable
Completed
Conditions
Dementia
Depression
Anxiety
Mental Health - Anxiety
Neurological - Dementias
Mental Health - Depression
Registration Number
ACTRN12618000241235
Lead Sponsor
Associate Professor Sunil Bhar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
269
Inclusion Criteria

Residents are eligible to participate if they:
1.are currently 65 years or older.
2. are currently living in residential aged care facilities
3.are diagnosed with dementia (major neurocognitive disorder, according to the Diagnostic and Statistical Manual of Mental Disorders, fifth edition [DSM 5]),
4.have within the six months been found to have mild to moderate cognitive impairment as defined as a score between 24 and 10 on the mini-mental state examination (MMSE) or the equivalent on the Psychogeriatric Assessment Scale Cognitive Impairment Scale (PAS-CIS) – 4 to 15 inclusive
5.have within the past year been found to have clinically significant levels of depression as indicated by a minimum of 7 on the Cornell Scale for Depression in Dementia (CSDD) or 11 on the Rating Anxiety in Dementia (RAID)

Family/friend caregivers will be eligible to participate if they are
1.nominated by the resident or legal proxy as an important source of care for the resident
2.are at least 18 years old, and
3.can communicate in English
4.willing to participate in project activities

Facility staff will be eligible to participate if they are
1.nominated by the resident, legal proxy or unit manager/clinical as an important source of care for the resident
2.are at least 18 years old, and
3.can communicate in English
4.willing to participate in project activities

Exclusion Criteria

Residents with limited capacity to communicate verbally in English (due to a lack of English language proficiency as assessed by facility or research staff) or who are unable to complete study procedures due to health conditions (e.g., resident is physically unwell, highly distressed)(as assessed by facility or research staff) will not be eligible to participate in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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