Effectiveness of a Multifactorial Intervention on Frailty

Not Applicable

Completed

• Conditions: Frail Elderly; Cognitive Impairment; Dependence
• Interventions: Other: Multifactorial intervention

• Registration Number: NCT01969526
• Lead Sponsor: Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina

Brief Summary

Objective: To evaluate the effectiveness of a multifactorial intervention program based on physical activity and diet, memory workshops and review of medication, to modify frailty parameters, muscle strength and physical and cognitive performance in people 65 years or older with a positive screening for frailty. Secondly, to assess changes in falls, hospitalizations, nutritional risk, disability and institutionalization or home-care.

Methods: randomized clinical trial with a control group, of one year and a half of follow-up, conducted in eight primary care teams in Barcelona. Individuals to be included are 65 years or older with positive frailty screening, timed get-up-and-go between 10 to 30 seconds, and cognitive Lobo test greater than or equal to 18. 165 patients will be selected in each group (difference to be detected on physical performance (Short physical performance battery (SPPB)): 0.5 units; common Standard Deviation : 1.42, 20% lost to follow-up).

Intervention: consists in three different actions on frailty dimensions, applied to each subject in the intervention group, in groups of 15 participants: rehabilitative therapy plus intake of hyperproteic shakes, memory workshop and review of the medication.

Evaluations will be blinded and conducted at 0, 3 and 18 months. Analysis of variance for repeated measures to adjust for differences attributable to intervention effect and for potential confounders such as comorbidity, sensory limitations, social risk, other medical or social interventions, among others.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01
• Study First Submitted: 2013-08-01
• Study First Submitted QC: 2013-10-21
• Study First Posted: 2013-10-25
• Primary Completion: 2016-12
• Status Verified: 2017-03
• Study Completion: 2017-09-30
• Last Update Submitted: 2017-11-08
• Last Update Posted: 2017-11-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 352

Inclusion Criteria

• Positive Barber screen
• Timed get-up-and-go 10 to 20 seconds
• cognitive Lobo test greater than or equal to 18

Exclusion Criteria

• Home Care
• Institutionalization
• Conditions not allowing physical exercise

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Multifactorial Intervention	Multifactorial intervention	Intervention consists in three different actions on frailty dimensions, applied to each subject in the intervention group, in groups of 15 participants: rehabilitative therapy plus intake of hyperproteic shakes, memory workshop and review of the medication.

Primary Outcome Measures

Name	Time	Method
Change from Baseline in Short Physical performance battery at 3 and 18 months	0,3,18 months	The Short Physical Performance Battery (SPPB) is a standardised assessment tool of lower limb function, testing 3 dimensions: standing balance, walking speed, and chair stands. Each component is scored between 0-4, total score from 0 (poor performance) to 12 (best performance).
Change from Baseline in Muscle strength at 3 and 18 months	0,3,18 months	Evaluation of upper extremities strength was assessed through the measurement of force with a handgrip dynamometer. Grip strength was evaluated using a portable hand dynamometer (JAMAR®0-90 kg, coding 506320). The participants were seated with their shoulder in a neutral position and their elbow flexed at 90°. Three attempts were performed alternately in each hand; the mean of the three measures was recorded.
Change from Baseline in Cognitive Performance (Barcelona test) at 3 and 18 months	0,3,18 months	The first neuro-psychometric instrument developed in Spain to measure semi-quantitatively cognitive status in clinical neurology was the Barcelona Test (BT). Shortened version of the BT, named Barcelona Test Review (BTR) had been used for neuropsychological area evaluation in our participants and it takes only 20-30 minutes to administer

Secondary Outcome Measures

Name	Time	Method
Change from Baseline in Functional Capacity at 18 months	18 months	Barthel Index Lawton\&Brody Index
Number of Participants Hospitalized during follow-up, at 18 months	18 months
Number of Participants with Falls during follow-up, at 18 months	18 months
Number of Participants Institutionalized during follow-up, at 18 months	18 months
Number of Participants included in Home Health care during follow-up, at 18 months	18 months

Trial Locations

Locations (1)

Institut Català de la Salut; 🇪🇸 Barcelona, Spain