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Improving anxiety assessment and management in people with cognitive impairment and dementia: Validation of an informant measure and pilot testing of a multi-component behavioural intervention.

In cognitively impaired patients, is a 12-week multi-component behavioural intervention effective in the treatment of anxiety.

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000364875
Enrollment
20
Registered
2012-03-29
Start date
2012-04-01
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

None listed

Brief summary

The aim of this pilot study is to determine the feasibility of a 12-week multi-component anxiety management program for the treatment of anxiety symptoms in people with cognitive impairment.

Interventions

This is a pilot study of a 12 week multi-component behavioural intervention for people with dementia with clinically significant anxiety. The behavioural intervention will engage both the person with dementia and an unpaid caregiver. Components will include psychoeducation, anxiety monitoring, relaxation training, activity scheduling, and a sleep intervention. The sleep intervention will provide participants with techniques to improve night-time sleep. The focus will be on helping family member

This is a pilot study of a 12 week multi-component behavioural intervention for people with dementia with clinically significant anxiety. The behavioural intervention will engage both the person with dementia and an unpaid caregiver. Components will include psychoeducation, anxiety monitoring, relaxation training, activity scheduling, and a sleep intervention. The sleep intervention will provide participants with techniques to improve night-time sleep. The focus will be on helping family members to better manage anxiety and associated behaviours. The program will be conducted by trained personnel. The sessions will be weekly and each session will last approximately 40 minutes.

Sponsors

University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

patients of RBWH memory clinic with cognitive impairment and significant anxiety symptoms informant who has regular contact with participant able to understand english at least 60 years of age

Exclusion criteria

patients without cognitive impairment patients without significant anxiety symptoms patients without suitable informant patients non-fluent in english under the age of 60

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026