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. Author manuscript; available in PMC: 2022 Nov 1.
Published in final edited form as: J Appl Gerontol. 2022 Jun 24;41(11):2316–2328. doi: 10.1177/07334648221111123

Table 2.

Instruments Collected at Baseline and Post-Intervention

Data Collection Timepoint Respondent Data Collection Method * Instrument
Baseline (1 week prior to intervention period) Caregiver Questionnaire CMAI
PSQI
ESS
QOL-AD – CG report**
CWBS
SF-12
Demographics form
Health History form
Interview NPI
RAID – CG report **
PWD Interview MoCA
RAID – PWD report **
QOL-AD – PWD report **
Post-Intervention (1 week after intervention period) Caregiver Questionnaire CMAI
PSQI
ESS
QOL-AD – CG report **
CWBS
SF-12
WBIAT – CG version
Health History Update
Interview NPI
RAID – CG report **
PWD Interview MoCA
RAID – PWD report **
QOL-AD – PWD report **
Questionnaire WBIAT – PwD version

Note. CG caregiver, CMAI Cohen-Mansfield Agitation Inventory-Relatives version, CWBS Caregiver Well-Being Scale, ESS Epworth Sleepiness Scale, MoCA Montreal Cognitive Assessment Test, NPI Neuropsychiatric Inventory, PWD person with dementia, RAID Rating Anxiety in Dementia Scale, SF-12 Optum SF-12v.2 Health Survey

*

Caregivers completed questionnaires electronically or by hardcopy based on their preference. Participants with dementia completed the WBIAT – PwD version by hardcopy questionnaire only. Interviews were conducted virtually or by telephone based on the participant preference.

**

The RAID and QOL-AD are both completed independently by self-report by the person with dementia and by the caregiver by proxy for the person with dementia. All other measures are completed by either the person with dementia, or the caregiver.