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. 2017 Nov 28;7(11):e018744. doi: 10.1136/bmjopen-2017-018744

Table 2.

SENSE-Cog SSI field trial schedule of events and assessments

Baseline SSI* Follow-up
Visit number / / 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Visit week −2 −1 0 1 2 3 4 5 6 7 8 9 10 11 12 13
Allowable visit window:+/−3 days
Identification X
Information X
Recruitment X
Informed consent X
Screening: HearCheck X
Screening: PEEK Acuity (Worldwide) X
Screening: visual field X
Screening: MoCA X
LV-VFQ-20 X A (A) X
HHIE-S X A (A) X
DEM-QOL X A (A) X
DEM-QOL-P X A (A) X
NPI X A (A) X
GSE X A (A) X
EQ-5D-5L X A (A) X
EQ-5D-5L-P X A (A) X
PHQ-15 X A (A) X
SF-12 X A (A) X
SF-12-P X A (A) X
GDS-15 X A (A) X
FCRS X A (A) X
BADLS X A (A) X
RSS X A (A) X
RUD-Lite baseline X
RUD-Lite follow-up A (A) X
Ophthalmological assessment† X
Audiological assessment† X
Glasses fitting X (X) (X)
Hearing aid fitting‡ X X (X) (X)
SST diary X X X X X X X X X X X X
PwD diary X X X X X X X X X X X X
SP diary X X X X X X X X X X X X
Sensory devices training X X (X) (X) (X) (X) (X) (X) (X) (X)
Functionality/usability of sensory devices X X X X X X X X X X X X
Communication training X (X) (X) (X) (X) (X) (X) (X) (X) (X)
Goal setting X (X)
Goal review X (X) (X) (X) (X) (X) (X) (X)
Goal outcome X (X) (X) (X) (X) (X)
Referral to clinical/social services X (X) (X) (X) (X) (X) (X) (X)
Provision of supplementary devices X (X) (X) (X) (X) (X) (X)
Develop hobbies, interests X (X) (X) (X) (X) (X)
Semistructured interview A X
Revisit and recap (F2F or phone)§ X X X X X

Key, X on this date; (X)—may take place/follow on, on this date; A—abbreviated intervention participants only; (A)—may take place/follow on at this date for abbreviated intervention participants.

*This details the process for the full intervention. The ‘abbreviated’ intervention will complete at week 3 with follow up assessments and follow-up interviews at week 4/5. The order of the SSI is flexible, depending on time to receive sensory equipment and participant’s needs.60

†Ophthalmological and audiological assessments will be conducted based on positive screening results. Not all participants will receive full clinical hearing and vision screening, if not required. Hearing aids and glasses are prescribed if deemed necessary by clinical assessment. Not all participants may require both hearing aid and glasses.

‡There may be a longer duration than 1 week between prescribing a hearing aid and receipt of hearing aid, depending if instant fit or moulded fit. The SST will undertake SSI visits during this time on weekly basis.

§Revisit and recap: these additional weeks of intervention allow for the SST to revisit and recap any of the previous components in more depth and to work on goal-setting and achievement activities with the person with dementia and study partner.

BADLS, Bristol Activities of Daily Living Scale47; DEM-QOL, Dementia Quality of Life31; DEMQOL-P, Dementia Quality of Life Proxy31; EQ-5D-5L-P, EuroQol 5 Dimensions 5 Levels Proxy55; EQ-5D-5L, EuroQol 5 Dimensions 5 Levels55; F2F, face to face; FCRS, Family Caregiving Role Scale61; GDS-15, Geriatric Depression Scale (15-item)62; GSE, Generalised Self-Efficacy Scale Chen63; HHIE-S, Hearing Handicap Inventory for the Elderly Screening Tool34); LV-VFQ-20, Low Vision Visual Functioning Questionnaire—20-item64; MoCA, Montreal Cognitive Assessment36; NPI, Neuropsychiatric Inventory Cummings65; PHQ-15, The Patient Health Questionnaire (15 item)60; PwD, person with dementia; RSS, Relationship Satisfaction Scale Burns66; RUD-Lite, Resource Utilisation in Dementia57; SF-12-P, 12-Item Short Form Survey Proxy56;56 SP, study partner; SSI, sensory support intervention; SST, Sensory Support Therapist.