Actively Recruiting
Effectiveness of 8 Week Multicomponent Exercise Program in Older Adults With Frailty and Cognitive Impairment
Led by University of Malaga · Updated on 2024-06-04
17
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Multicomponent exercise program in a frail population. It is analyzed whether there is an improvement in different parameters of the daily life of the study subjects, analyzing the variables of: physical condition, fragility, balance, quality of life, upper limb strength, autonomy, cognitive state and depression.
CONDITIONS
Official Title
Effectiveness of 8 Week Multicomponent Exercise Program in Older Adults With Frailty and Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults over 65 years of age
- Have frailty according to the Short Physical Performance Battery
- Ability to walk independently or with external aids
- Score of 15 or higher on the Lobo Mini Cognitive Examination (MEC-35)
- Patients with resolved hip fracture or Parkinson's disease
- Motivated and committed to participate and able to sign informed consent
You will not qualify if you...
- Adults under 65 years of age
- No frailty or unable to walk independently or with aids
- Score less than 15 on the Lobo Mini Cognitive Examination indicating serious cognitive or emotional impairment
- Currently treated with tranquilizers, sedatives, non-diuretic hypotensive agents, or antidepressants
- Diagnosis of amyotrophic lateral sclerosis, multiple sclerosis, diabetic neuropathy, or severe sensory deficit
- Lack of motivation or interest in participation
- Refusal to sign informed consent and report sheet
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cristian Carmona Cantalejo
Estación de Cártama, Málaga, Spain, 29580
Actively Recruiting
Research Team
C
Cristian Carmona Cantalejo
CONTACT
R
Rocío Martín Valero, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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