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NCT05007353Completed

The SINgapore GERiatric Intervention Study to Reduce Cognitive Decline and Physical Frailty (SINGER) Study

The SINgapore GERiatric Intervention Study to Reduce Cognitive Decline and Physical Frailty (SINGER) Study, Biomarker and Health Service Research Analyses

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

A study in Finland found that a multidomain intervention of physical activity, nutritional guidance, cognitive training, social activities and management of vascular risk factors slowed cognitive decline in healthy older adults at increased risk of cognitive decline. A 6-month pilot study was initiated in Singapore, which demonstrated the cultural feasibility and practicality of the FINGER interventions and a set of locally adapted interventions in an Asian population. The SINGER study is a 2-year randomized controlled trial that aims to test the efficacy and safety of these lifestyle changes, including diet and cardiovascular risk factor management, cognitive and physical exercises, in delaying cognitive decline in older adults at risk of dementia.

Status (registry)
Completed
Study type
Interventional
Enrollment
1212 (actual)
First submitted
28 Jul 2021
Start date
Aug 2021
Primary completion date
Dec 2025
Lead sponsor
National University of Singapore
NCT number
NCT05007353

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1212
  • From Aug 2021 to the primary completion date, Dec 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • malignant diseases
  • dementia
  • symptomatic cardiovascular disease
  • other conditions inhibiting from safe engagement in the prescribed intervention and other conditions preventing cooperation, as judged by the study physician

Other

  • major depression
  • revascularisation within 1 year
  • severe loss of vision, hearing or communicative ability

Who the study is looking for

  • Age 60-80 years
  • Able to understand English/Chinese
  • Risk of dementia: Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE) dementia risk score ≥6 indicating the presence of modifiable risk factors Modifiable lifestyle factors (fulfilling at least one of the following LIBRA index for diet, cognitive activity, physical activity)
  • Cognitive performance at the mean level or slightly lower than expected for age (MoCA ≥18, ≤27)
  • No plans to travel outside of Singapore for an extended period of time over the course of the study
  • Free of physical disabilities that preclude participation in the study
  • Willing to complete all study-related activities for 24 months
  • Willing to be randomized to either lifestyle intervention group

Age in the registry: 60 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Neuroscience Institute @ Tan Tock Seng Campus (NNI @ TTSH campus)
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status
National University Hospital
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status
National University of Singapore, Yong Loo Lin School of Medicine
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.