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Dutch Multidomain Lifestyle Intervention in Older Adults at Risk of Cognitive Decline

Dutch Multidomain Lifestyle Intervention in Older Adults at Risk of Cognitive Decline

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05256199
Acronym
FINGER-NL
Enrollment
1210
Registered
2022-02-25
Start date
2022-02-24
Completion date
2027-08-01
Last updated
2026-06-02

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

Conditions

Cognitive Decline, Life Style, Risk Reduction

Brief summary

FINGER-NL is a multi-center, randomized, controlled, multidomain lifestyle intervention trial among 1,206 older adults at risk for cognitive decline with a duration of 24 months. Participants are randomized in a 1:1 ratio to a personalized multi-domain lifestyle intervention (high-intensity intervention group) versus online access to general lifestyle-related health information (low-intensity intervention group). After the intervention period, participants are invited for a 24 month extension of follow-up.

Interventions

A multidomain lifestyle intervention, including (1) physical activity, (2) cognitive training, (3) cardiovascular risk factor management (Cardiovascular), (4) dietary counselling, (5) Souvenaid, (6) sleep counselling, (7) stress management, and (8) social activities.

Sponsors

Alzheimercentrum Amsterdam
Lead SponsorOTHER
Maastricht University
CollaboratorOTHER
Radboud University Medical Center
CollaboratorOTHER
Wageningen University and Research
CollaboratorOTHER
University Medical Center Groningen
CollaboratorOTHER
Danone Nutricia Research
CollaboratorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* 60-79 years of age at pre-screening; * Adequate fluency in Dutch to understand the informed consent and complete questionnaires; * Providing informed consent to all study procedures; * Internet access at home; * Presence of ≥3 self-reported risk factors for cognitive decline (must contain at least 2 modifiable risk factors and 1 non-modifiable riskfactor).

Exclusion criteria

* Diagnosis of dementia or mild cognitive impairment at baseline (self-reported); * Significant cognitive impairment assessed using the Modified Telephone Interview for Cognitive Status battery (TICSm score\<23); * Conditions affecting safe and continuous engagement in the intervention (e.g. under treatment for current malignant diseases, major psychiatric disorders (e.g. major depression, psychosis, bipolar disorder), neurological disorders (e.g. Parkinson's disease, multiple sclerosis), symptomatic cardiovascular disease (e.g. stroke, angina pectoris, heart failure, myocardial infarction), re-vascularization within three months, severe loss of vision, hearing or communicative ability, severe mobility impairment, other conditions preventing co-operation) as judged by the local study nurse or consulted physician at the local study site; * Coincident participation in any other intervention trial at time of pre-screening. * Coincident participation of spouse in FINGER-NL trial.

Design outcomes

Primary

MeasureTime frameDescription
2-year change from baseline in global cognitive composite score2 years (measured at baseline, follow-up 1 and follow-up 2)Global cognitive composite score derived from subtest scores from the Neuropsychological Test Battery (NTB) that includes 15-Word Verbal Learning Test delayed recall (discrete number; 0-15 (higher score means a better outcome)), Digit Symbol Substitution Test 90 seconds (discrete number; 0-90 (higher score means a better outcome)), WAIS digit span backwards (discrete number; 0-14 (higher score means a better outcome)), and semantic fluency (discrete number; 0-no maximum, higher score means a better outcome)).

Secondary

MeasureTime frameDescription
15-Word Verbal Learning Test delayed recall2 years (measured at baseline, follow-up 1 and follow-up 2)discrete number; score: 0-15 (higher score means a better outcome)
Digit Symbol Substitution Test 90 seconds2 years (measured at baseline, follow-up 1 and follow-up 2)discrete number; 0-90 (higher score means a better outcome)
Wechsler Adult Intelligence Scale (WAIS) digit span backwards2 years (measured at baseline, follow-up 1 and follow-up 2)discrete number; 0-14 (higher score means a better outcome)
Semantic fluency2 years (measured at baseline, follow-up 1 and follow-up 2)word count in one minute; minimum 0, no maximum, higher score means a better outcome.
Instrumental activities of daily living using the Amsterdam Instrumental Activity of Daily Living Questionnaire (A-IADL-Q)2 years (measured at baseline, follow-up 1 and follow-up 2)Total scores range approximately 20-70, higher scores indicate better IADL functioning
5 level EuroQol-5D (EQ-5D-5L)2 years (measured at baseline, follow-up 1 and follow-up 2)Quality of life, score 0-100, higher scores indicate better quality of life
LIfestyle for BRAin health (LIBRA)2 years (measured at baseline, follow-up 1 and follow-up 2)Modifiable dementia risk using lifestyle for brain health; The score ranges from -5.9 (minimum score) to +12.7 (maximum score), with higher scores meaning a worse outcome (higher dementia risk)
grip strength test2 years (measured at baseline, follow-up 1 and follow-up 2)Scores between 0 to 90 kg can be measured on the Jamar Hand dynamometer, with higher scores indicating better grip strength
SQUASH questionnaire2 years (measured at baseline, follow-up 1 and follow-up 2)METs derived from the Ainsworth's compendium of physical activity will be used to classify physical activity intensity (\<1.5METs- sedentary, 1.6-2.9 METs- light, 3.0-5.9METs- moderate, \>6.0- vigorous physical activity).
LASA Sedentary Behavior Questionnaire2 years (measured at baseline, follow-up 1 and follow-up 2)Average hours and minutes of sedentary behavior a day, range from 0 to 24 hours. Higher scores (more hours) means a more sedentary behavior.
Pittsburgh Fatigability Scale2 years (measured at baseline, follow-up 1 and follow-up 2)Total physical and mental fatigability scores range from 0-50, with higher scores indicating higher fatigability.
SARC-F Sarcopenia Questionnaire2 years (measured at baseline, follow-up 1 and follow-up 2)sarcopenia, scores range from 0 to 10 (i.e. 0-2 points for each component; 0 = best to 10 = worst).
Five Facet Mindfulness Questionnaire - Short Form (FFMQ-SF)2 years (measured at baseline, follow-up 1 and follow-up 2)Total scale ranges from 24 - 120, higher scores indicate more mindfulness
Perceived Stress Scale2 years (measured at baseline, follow-up 1 and follow-up 2)Total score, scale 0 - 40, higher scores indicate more perceived stress
MetaMemory in Adulthood (MIA)2 years (measured at baseline, follow-up 1 and follow-up 2)Sum of Part 1 + Part 2A and B. Part 1: Strategy (scores 10 - 50, higher scores indicate more use of strategies), Part 2A: Subjective memory functioning, scores ranges from 23 - 115, with higher scores indicate better memory self-efficacy and 2B: Locus, scores ranges from 7 - 35, higher scores indicate better perceived personal control over remembering abilities.
Blood pressure2 years (measured at baseline, follow-up 1 and follow-up 2)scores range from approximately (for diastolic) 60-120 and (for systolic) 100-180 mmHg, with higher scores indicating higher blood pressure.
Cholesterol2 years (measured at baseline, follow-up 1 and follow-up 2)total (healthy level: 125 to 200mg/dL), HDL (healthy level = 40mg/dL or higher), LDL (healthy level = Less than 100mg/dL) + triglycerides (healthy level = less than 150-199 mg/dL)
Blood glucose2 years (measured at baseline, follow-up 1 and follow-up 2)HbA1C, scores range from approximately 30-100 mmol/mol, with higher scores indicate higher blood glucose levels.
Waist circumference2 years (measured at baseline, follow-up 1 and follow-up 2)measured in cm
Hip circumference2 years (measured at baseline, follow-up 1 and follow-up 2)measured in cm
Height2 years (measured at baseline, follow-up 1 and follow-up 2)measured in cm
Weight2 years (measured at baseline, follow-up 1 and follow-up 2)measured in kg
Hill-Bone Medication Adherence Scale2 years (measured at baseline, follow-up 1 and follow-up 2)scores range from 9-26, with lower scores indicating better medication adherence
MIND-adjusted Eetscore-FFQ2 years (measured at baseline, follow-up 1 and follow-up 2)Dutch Healthy Diet Index 2015 score (range 0-160 points, higher scores mean better outcome) and MIND score (range 0-15 points, higher scores mean better outcome), assessed by a short Food Frequency Questionnaire.
Nutritional intake2 years (measured at baseline, follow-up 1 and follow-up 2)Change in nutritional intake measured by an online 3-day food diary (assessed by Traqq application), qualitative assessment
Pittsburg Sleep Quality Index2 years (measured at baseline, follow-up 1 and follow-up 2)Total score ranging from 0 to 21 with the higher total score (referred to as global score) indicating worse sleep quality
Insomnia severity index2 years (measured at baseline, follow-up 1 and follow-up 2)The score ranges from 0 (minimum score) to 28 (maximum score), with lower scores indicating a better outcome
Lubben Social Network Scale2 years (measured at baseline, follow-up 1 and follow-up 2)The score ranges from 0 (minimum score) to 30 (maximum score), with higher scores meaning a better outcome (higher level of perceived social support)
De Jong Gierveldt Loneliness Scale2 years (measured at baseline and follow-up 2)The score ranges from 0 (minimum score) to 6 (maximum score), with higher scores representing a worse outcome (higher loneliness scores)
Aβ42/40 ratio2 years (measured at baseline and follow-up 2)amyloid-β (1-42)/(1-40) (pg/mL)
p-tau2 years (measured at baseline and follow-up 2)phosphorylated tau (pg/mL)
NfL2 years (measured at baseline and follow-up 2)neurofilament light chain (pg/mL)
GFAP2 years (measured at baseline and follow-up 2)glial fibrillary acidic protein (pg/mL)
BDNF2 years (measured at baseline and follow-up 2)brain-derived neurotrophic factor (pg/mL)
Actigraph (Groningen site only)2 year (measured for 1 week at baseline, follow-up 1 and follow-up 2)physical activity, sedentary behavior and sleep-wake activity
Physical Activity Record questionnaire (Groningen site only)2 year (measured for 1 week at baseline, follow-up 1 and follow-up 2)physical activity, sedentary behavior and sleep-wake activity

Countries

Netherlands

Contacts

PRINCIPAL_INVESTIGATORMarissa D. Zwan, Dr.

Alzheimer Center Amsterdam

PRINCIPAL_INVESTIGATORSebastian Köhler, Prof.

Maastricht University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 3, 2026