Pre-Frail or Frail State
Conditions
Brief summary
The aims of this proposed community-based randomized controlled trial are to evaluate the effectiveness of nutritional, physical exercise and cognitive training interventions for at-risk and frail elderly, to elucidate the biological determinants and changes associated with frailty, and to develop, evaluate and demonstrate the feasibility of screening instruments for frailty.
Detailed description
Community-living elderly persons are screened and 250 participants satisfying rigorous criteria for frailty are randomized to received nutritional, physical training, cognitive training, combined or control arms for 24 weeks and followed up for 12 months. Baseline evaluations will include an extensive range of potential markers of frailty and outcome measures, including functional disability and hospitalizations. Frail subjects who were selected for the interventional trial (N=250) are followed up at 3, 6 and 12 months after baseline assessment. Non-trial subjects (about 2750) are followed up at 1 year after baseline assessment
Interventions
DIETARY_SUPPLEMENTNutritional Intervention
Each subject in the nutritional intervention group is provided with a commercial liquid formula (Fortisip Multi Fibre, Nutricia), which should be taken every evening for a period of 24 weeks. Subjects are also given one capsule of iron and folate supplement (Sangobion, Merck; consisting of 1 mg folate and 29mg iron), one capsule of Vitamin B6 and vitamin B12 supplement (Neuroforte; consisting of 200mcg B12 and 200mg vit B6) and one tablet of Caltrate with Vitamin D (consisting of 200 IU vitamin D and 600 mg of calcium) for a duration of 24 weeks.
OTHERPhysical Exercise
The exercise intervention group comprises a combination of 2 types of exercise: resistance exercise and in-balance exercise. Key components in both programs are balance and strength, because these are the most prominent domains that should be addressed in at risk frail elderly. The first program is administered in the first 6-week, and then followed by the second program for the next 6-week of intervention period. Both exercise programmes are tailored to the functional needs of the participants, maintaining a moderate intensity that focuses on long-term sustainability and enjoyment.
OTHERCognitive Training
The proposed cognitive training intervention program comprises: 1. Reasoning training focusing on inductive reasoning, the ability to solve problems that follow a serial pattern and manifest in executive functioning. 2. Memory training focusing on verbal episodic memory, which deals with acquisition and retrieval of information acquired in a particular place at a particular time. 3. Speed training focusing on visual search and the ability to identify and locate visual information quickly in a divided attention format, with and without distractors.
OTHERCombined
Nutritional Intervention + Physical Exercise + Cognitive Training
OTHERPlacebo
Participants will receive their usual diet and placeboes.
Sponsors
National University of Singapore
Alexandra Hospital
St Luke's Hospital, Singapore
National Medical Research Council (NMRC), Singapore
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
65 Years to 89 Years
Healthy volunteers
Yes
Inclusion criteria
1. Age of 65 years or older 2. Living at home 3. Able to walk without personal assistance and no other physical limitations that can limit participation and adherence, particularly to exercise intervention programme 4. Meet criteria for frailty Operational definition of frailty. The participants are assessed and classified on the level of frailty by the following measures and criteria: 1. Weight loss 2. Slowness 3. Poor balance and weakness assessed by chair stand test 4. Muscle weakness assessed by hand grip and knee extension strength 5. Exhaustion, fatigue or low endurance 6. Low physical activity
Exclusion criteria
1. Member of household already enrolled 2. Dementia or cognitive impairment, major depression or other psychotic disorders 3. Severe audio-visual impairment 4. Progressive, degenerative neurologic disease like Parkinsonism, fits/ epilepsy, etc 5. Rapidly progressive or terminal illness under palliative care with life expectancy less than 12 months 6. History of alcohol abuse or any other substance abuse 7. Severely affect muscle/joint dysfunction resulting in disability 8. Hospital admission in the past 3 months 9. Regular physical training or physiotherapy or current participation in a vigorous exercise or weight-training program more than once per week 10. Undergoing therapeutic diet incompatible with nutritional supplementation 11. In the opinion of research clinician, the intervention is deemed to be potentially hazardous for the subject, such as serious cardiac and pulmonary disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of frailty | 12 months |
| Frailty score (continuous variable) | 12 months |
| Measures of frailty components (BMI, fast gait speed test, knee extension, exhaustion score and time spent on physical activities per day). | 12 months |
Secondary
| Measure | Time frame |
|---|---|
| Frequency of falls (defined as an event resulting in a person coming to rest unintentionally on the ground or other lower level; near-falls are not included; Robertson, 2001). | 12 months |
| Disability in activities of daily living (ADL) and instrumental activities of daily living (IADL). | 12 months |
| Health service utilization (frequencies of doctor visits, emergency room visit, hospitalization, nursing home admission) | 12 months |
| Mortality | 12 months |
Countries
Singapore
Outcome results
None listed