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Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01041989
Recruitment Status : Active, not recruiting
First Posted : January 5, 2010
Last Update Posted : April 19, 2023
Sponsor:
Collaborators:
Academy of Finland
University of Helsinki
University of Eastern Finland
University of Oulu
Kuopio Research Institute of Exercise Medicine
Western University, Canada
Karolinska Institutet
Umeå University
Information provided by (Responsible Party):
Miia Kivipelto, Finnish Institute for Health and Welfare

Brief Summary:
This multi-center (6 sites: Helsinki, Kuopio, Oulu, Seinäjoki, Turku, Vantaa) intervention study aims to prevent cognitive impairment, dementia and disability in 60-77 year old persons at an increased dementia risk. The 2-year multi-domain life-style intervention includes nutritional guidance, exercise, cognitive training, increased social activity, and intensive monitoring and management of metabolic and vascular risk factors. The primary outcome is cognitive impairment measured by a sensitive Neuropsychological Test Battery (NTB), and Stroop and Trail Making tests to capture early cognitive impairment typical for both Alzheimer's disease and vascular dementia. We hypothesize that the multi-domain intervention will reduce cognitive impairment in the study group compared to the control group during the initial 2-year intervention period and reduce dementia incidence after the extended follow-up (until at least 300 participants have developed dementia).

Condition or disease Intervention/treatment Phase
Cognitive Impairment Dementia Behavioral: Nutritional guidance Behavioral: Exercise Behavioral: Cognitive training Other: Reduction of vascular risk factors Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1200 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability
Study Start Date : September 2009
Actual Primary Completion Date : December 2013
Estimated Study Completion Date : December 2025

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dementia

Arm Intervention/treatment
No Intervention: Standard health counseling at baseline
Experimental: Lifestyle counseling
Multi-domain lifestyle counseling including nutritional guidance, increased physical activity, cognitive training, increased social activity and intensive monitoring of vascular and metabolic risk factors.
Behavioral: Nutritional guidance
Individual counseling sessions and group meetings will be organized.

Behavioral: Exercise
Guided muscle strength training and aerobic exercise.

Behavioral: Cognitive training
Cognitive training will be implemented through 8 group sessions lead by a psychologist and a computer-based cognitive training program available to participants via the internet.

Other: Reduction of vascular risk factors
Monitoring and maintenance of metabolic and vascular risk factors




Primary Outcome Measures :
  1. Cognitive impairment assessed with a Neuropsychological Test Battery, and Stroop and Trail Making tests. [ Time Frame: 2 years ]

Secondary Outcome Measures :
  1. Depressive symptoms will be assessed using the Zung depression scale. [ Time Frame: 2 years ]
  2. Disability will be assessed using the ADCS-ADL scale [ Time Frame: 2 years ]
  3. Quality of Life will be assessed using the RAND-36 and 15D questionnaires. [ Time Frame: 2 years ]
  4. Utilization of health resources will be assessed using questionnaire and register data. [ Time Frame: 2 years ]
  5. Vascular and metabolic risk factors will be assessed with blood pressure and anthropometric measurements, and laboratory analyses of metabolic biomarkers. [ Time Frame: 2 years ]
  6. Vascular and metabolic morbidity and mortality will be assessed through questionnaire and register data. [ Time Frame: 2 years ]
  7. Changes in dietary biomarker levels will be assessed through laboratory testing. [ Time Frame: 2 years ]


Information from the National Library of Medicine

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Ages Eligible for Study:   60 Years to 77 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • aged 60-77 years
  • dementia Risk Score 6 points or more
  • fulfillment of at least one of the following CERAD criteria: i) MMSE: 20-26 points ii) word list memory task (3x10 words): 19 words or less iii) delayed recall: 75% or less

Exclusion Criteria:

  • malignant diseases
  • dementia
  • substantial cognitive decline
  • major depression
  • symptomatic cardiovascular disease
  • revascularisation within 1 year
  • severe loss of vision, hearing or communicative ability
  • other conditions inhibiting from safe engagement in the prescribed intervention as judged by the study physician
  • other conditions preventing from cooperation as judged by the study physician

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01041989


Locations
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Finland
Finnish Institute for Health and Welfare
Helsinki, Finland, 00300
University of Eastern Finland
Kuopio, Finland, 70211
University of Oulu
Oulu, Finland, 90014
Research Center Mediwest
Seinajoki, Finland, 60220
Finnish Institute for Health and Welfare
Turku, Finland, 20720
Sponsors and Collaborators
Finnish Institute for Health and Welfare
Academy of Finland
University of Helsinki
University of Eastern Finland
University of Oulu
Kuopio Research Institute of Exercise Medicine
Western University, Canada
Karolinska Institutet
Umeå University
Investigators
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Principal Investigator: Miia Kivipelto, professor Finnish Institute for Health and Welfare
Study Director: Tiina K Laatikainen, professor Finnish Institute for Health and Welfare
Study Director: Hilkka S Soininen, professor University of Eastern Finland
Study Director: Jaakko Tuomilehto, professor University of Helsinki
Study Director: Timo E Strandberg, professor University of Oulu
Study Director: Raimo Sulkava, professor University of Eastern Finland
Study Director: Rainer Rauramaa, professor Kuopio Research Institute of Exercise Medicine
Study Director: Antti Jula, research prof Finnish Institute for Health and Welfare
Study Director: Markku Peltonen, research professor Finnish Institute for Health and Welfare
Study Director: Satu Havulinna, PhD Finnish Institute for Health and Welfare
Study Director: Jaana Lindström, Adjunct prof. Finnish Institute for Health and Welfare
Study Director: Riitta Antikainen, professor Oulu City Health Services
Study Director: Tiia Ngandu, MD, PhD, Adjunct professor Finnish Institute for Health and Welfare
Study Director: Tuomo Hänninen, Adjunct prof University of Eastern Finland
Study Director: Jenni Lehtisalo, PhD Finnish Institute for Health and Welfare
Study Director: Alina Solomon, MD, PhD, Adjunct professor University of Eastern Finland
Publications of Results:
Strandberg TE, Levälahti E, Ngandu T, Solomon A, M Kivipelto for FINGER Study Group. Health-Related Quality of Life in a Multidomain Intervention Trial to Prevent Cognitive Decline (FINGER). Eur Ger Med. 2017; 8: 164-167.

Other Publications:

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Miia Kivipelto, Professor, Finnish Institute for Health and Welfare
ClinicalTrials.gov Identifier: NCT01041989    
Other Study ID Numbers: THL/TUET 122/2009
First Posted: January 5, 2010    Key Record Dates
Last Update Posted: April 19, 2023
Last Verified: April 2023
Keywords provided by Miia Kivipelto, Finnish Institute for Health and Welfare:
dementia
cognitive impairment
disability
intervention
elderly
lifestyle counseling
Additional relevant MeSH terms:
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Dementia
Cognitive Dysfunction
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurocognitive Disorders
Mental Disorders
Cognition Disorders