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Agility Training for Older Adults to Improve Fall Risk Factors

Agility Training for Older Adults: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05727254
Acronym
AgilE
Enrollment
48
Registered
2023-02-14
Start date
2022-07-13
Completion date
2023-12-15
Last updated
2025-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Age-Related Loss of Skeletal Muscle Mass, Aging, Sarcopenia, Cognitive Decline

Brief summary

In this randomized controlled trial the effect of 4 months of multi-component (strength, balance, cognition, endurance) exercise training intervention on measures of neuromuscular performance, cognition, and endurance as well as neural adaptations on a central and peripheral level is investigated. 40 subjects are recruited that are generally health and between 60 and 80 years of age. The interventions is based around exercises, where different tasks have to be solved simultaneously rather than serially, as has previously been done.

Interventions

Multi-component (strength, balance, cognition) exercise training.

Participants are being given the standard recommendations how much exercise and what type older adults should do.

BEHAVIORALExercise diary

Participants are instructed to write down their physical activity and exercises.

Sponsors

Oliver Faude
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Due to the nature of the study (exercise intervention) no masking of participants and intervention providers is possible.

Intervention model description

Randomized controlled trial with an intervention and a control arm.

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* willing to be randomized to either arm * ability to travel to the sports facility twice a week * understanding the german language

Exclusion criteria

* smoking, obesity * history of cardiovascular, pulmonary or chronic inflammatory disease * vision impairments * orthopaedic problems preventing them from participating in an exercise program * history of osteoporosis or recent low trauma fracture * less than two weeks during the intervention period * not have taken part in a structured exercise program more than once a week in the past three months

Design outcomes

Primary

MeasureTime frameDescription
Isometric knee-extension strength16 weeksStrength in torque (N\*m) of the quadriceps femoris muscle. Measured on an isokinetic device in an isometric condition.

Secondary

MeasureTime frameDescription
Blood Pressure16 weeksBlood pressure cuff on the right arm at the height of the aorta. Measured in mmHG.
Isometric knee-flexion strength16 weeksStrength in torque (N\*m) of the hamstring muscle group measured on an isokinetic device in an isometric condition.
Cognitive Processing Speed16 weeksEriksen flanker task performance measured be reaction speed in milliseconds and accuracy in percentage.
Cognitive Impulsiveness16 weeksGo / No-Go task performance measured by reaction speed in milliseconds and accuracy in percentage.
Balance Performance16 weeksStaying as stable as possible during ten seconds in tandem stance eyes open condition. Center of pressure sway path length in mm and average sway speed in m/s is calculated.
Hand Grip Strength16 weeksUsing a handheld dynamometer with an extended arm squeezing as hard as possible. Measured in N.
Counter movement jump power16 weeksMeasured on a force plate participants are instructed to jump as high as possible with their hands akimbo. Peak of the time-power curve in Watts.
Stress16 weeks10 item qestionnaire (Perceived Stress Scale). Every answer is rated on a scale from 1 to 5.
Depression16 weeks15 item questionnaire (Center for Epidemiological Studies Depression Scale). Every answer is rated on a scale from 1 to 4.
Pulse Wave Velocity16 weeksEstimated from a mobile blood pressure cuff (mobil-O-graph) on the right arm. Measured in m/s.
Retinal vessel diameter16 weeksA photo is made from the retinal vessels with a static vessel analyzer (camera)through the eye and the vessel diameters are measured in mikrometers.
Quality of Life Questionnaire16 weeks26 item questionnaire (WHOQOL-Bref). Every answer is rated on a scale from 1 to 5. Aggregate Score from 0 to 100.
Fall Efficacy16 weeks16 item qestionnaire (Fall Efficacy Scale). Every answer is rated on a scale from 1 to 4.
Sleep Disturbances16 weeks7 item questionnaire (Insomnia Severity Index). Every answer is rated on a scale from 1 to 5.

Other

MeasureTime frameDescription
Corticospinal Inhibition16 weeksDifference between paired and single pulse motor evoked potential by transcranial magnetic stimulation.
Voluntary activation16 weeksDegree of ability to contract the soleus muscle voluntarily.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026