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Trial registered on ANZCTR


Registration number
ACTRN12617000007336
Ethics application status
Approved
Date submitted
10/11/2016
Date registered
3/01/2017
Date last updated
3/01/2017
Type of registration
Retrospectively registered

Titles & IDs
Public title
A supervised walking program to reduce risky wandering in people with severe dementia in residential aged care: A feasibility study
Scientific title
A supervised walking program to reduce risky wandering in people with severe dementia in residential aged care: A feasibility study
Secondary ID [1] 290513 0
None
Universal Trial Number (UTN)
U1111-1189-6932
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
dementia 300918 0
Wandering 300919 0
Condition category
Condition code
Neurological 300731 300731 0 0
Alzheimer's disease
Neurological 301153 301153 0 0
Dementias

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Participants will be taken for a walk by a care staff member or research assistant. Both received 2 hours of training from the principle investigator covering the intervention protocol and acceptable communication styles to be used while walking with participants. Communication style was limited to prescriptive, informative and supportive language to minimise the potential of confounding results with social communication. At the end of the training session the participating care staff and research assistant completed a quiz to assess understanding of communication styles with > 98% accuracy. The intervention protocol involved taking the participating person with dementia on a 30 minute walk, 30 minutes before their unique peak activity period, 5 days per week (Mon-Fri) for 3 weeks. The walk will be on a predetermined route either within the secure facility or outside the secure facility dependent upon care needs. To measure protocol fidelity, the person leading the walk completed a checklist of essential protocol items (pre walk checklist (asked to go for walk, wearing appropriate clothing, elimination needs attended to, offered a drink), time walk started, duration of walk, route taken, and comments about deviations from protocol). 10% of all interventions were observed by the principle investigator or project manager for inter rater reliability and to monitor communication styles.
Intervention code [1] 296366 0
Prevention
Intervention code [2] 296703 0
Behaviour
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 300139 0
Number of walks completed - recorded on fidelity check list completed at the end of each supervised walk by the person supervising the walk
Timepoint [1] 300139 0
Checklist was completed at the end of each supervised walk
Primary outcome [2] 300140 0
Congruence with intervention protocol
Timepoint [2] 300140 0
Checklist completed at the end of each supervised walk and checked by a second observer for 10% of all walks
Secondary outcome [1] 329176 0
Composite secondary outcome
Wandering characteristics - steps taken (Actigraph data), Frequency and duration of intrusion of private space (direct observation), type of pattern (lapping, pacing, random, direct) of ambulation (direct observation)
Timepoint [1] 329176 0
Pre (week 1), during (weeks 2-4) and post (week 5) intervention measures - 2 x 2hours / person / week
10% of all observations are checked by a second observer for IRR
Secondary outcome [2] 329177 0
Agitation - Cohen-Mansfield Agitation Inventory
Timepoint [2] 329177 0
Baseline (1 week before intervention), weeks 1-3 of the 3 week intervention, and a week after the 3 week intervention period
Secondary outcome [3] 329178 0
Sleep using General Sleep Scale
Timepoint [3] 329178 0
Baseline (1 week before intervention), weeks 1-3 of the 3 week intervention, and a week after the 3 week intervention period
Secondary outcome [4] 329179 0
Quality of Life using QoL-AD proxy report
Timepoint [4] 329179 0
Baseline (1 week before intervention), weeks 1-3 of the 3 week intervention, and a week after the 3 week intervention period
Secondary outcome [5] 329180 0
Falls as reported in facility incident reporting system
Timepoint [5] 329180 0
3 months before intervention commencement, weeks 1-3 of the 3 week intervention, and a week after the 3 week intervention period
Secondary outcome [6] 329181 0
weight
Timepoint [6] 329181 0
weekly weight collected at baseline (1 week before intervention), weeks 1-3 of the 3 week intervention, and a week after the 3 week intervention period

Eligibility
Key inclusion criteria
>65 years
Severe dementia as documented in medical file and confirmed using Modified Mini Mental State Exam
Independently ambulant (wheelie walker and walking stick acceptable)
Not acutely mentally ill
Positive wandering history as reported by care staff and confirmed using the Revised Algase Wandering Scale
Minimum age
65 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
<65 year
Not severe dementia
Not independently ambulant

Study design
Purpose of the study
Prevention
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Pre and post measures to examine impact of intervention on outcome measures
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Repeated measures ANOVA

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment postcode(s) [1] 14586 0
4020 - Scarborough
Recruitment postcode(s) [2] 14585 0
4022 - Rothwell

Funding & Sponsors
Funding source category [1] 294927 0
Other Collaborative groups
Name [1] 294927 0
Dementia Collaborative Research Centre
Country [1] 294927 0
Australia
Primary sponsor type
University
Name
Queensland University Of Technology
Address
Victoria Park Rd
Kelvin Grove, Qld, 4059
Country
Australia
Secondary sponsor category [1] 293760 0
None
Name [1] 293760 0
Address [1] 293760 0
Country [1] 293760 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 296303 0
Queensland University of Technology Human Research Ethics Committee
Ethics committee address [1] 296303 0
Ethics committee country [1] 296303 0
Australia
Date submitted for ethics approval [1] 296303 0
14/04/2015
Approval date [1] 296303 0
23/07/2015
Ethics approval number [1] 296303 0
1500000422

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 70378 0
Dr Margaret MacAndrew
Address 70378 0
QUT
Victoria Park Rd
Kelvin Grove, Qld, 4059
Country 70378 0
Australia
Phone 70378 0
+61 7 3138 5956
Fax 70378 0
Email 70378 0
margaret.macandrew@qut.edu.au
Contact person for public queries
Name 70379 0
Margaret MacAndrew
Address 70379 0
QUT
Victoria Park Rd
Kelvin Grove, Qld, 4059
Country 70379 0
Australia
Phone 70379 0
+61 7 3138 5956
Fax 70379 0
Email 70379 0
margaret.macandrew@qut.edu.au
Contact person for scientific queries
Name 70380 0
Margaret MacAndrew
Address 70380 0
QUT
Victoria Park Rd
Kelvin Grove, Qld, 4059
Country 70380 0
Australia
Phone 70380 0
+61 7 3138 5956
Fax 70380 0
Email 70380 0
margaret.macandrew@qut.edu.au

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.