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Fit in the Aged by Professional Training (FiAT)

U

University of Erlangen-Nürnberg Medical School

Status

Completed

Conditions

Frailty
Sarcopenia

Treatments

Other: Control
Procedure: Power Training
Procedure: Strength Training

Study type

Interventional

Funder types

Other

Identifiers

NCT00783159
32.5.8051.0113.0

Details and patient eligibility

About

This intervention study tests training methods to stabilize or improve functionality in the high risk group of prefrail elderly persons.

Full description

This study aims at the improvement of muscular function by physical exercise in prefrail elderly persons. Prefrail participants are recruited according to the frailty score of Fried. Taking into account, that vitamin D supplementation reduces falls and improves muscle strength in older people, all participants are supplemented by vitamin D. Two different training methods are tested.

After a run-in period of supplementation of vitamin D for two months, participants will be randomized into three different equally sized groups (n=25): Group A will receive power training. Group B will have progressive strength training. Group C will serve as a control group. They will receive a consultation about leading a healthy life with special attention being paid to nutrition and physical activity. The intervention period lasts for 12 weeks. The 60 minutes training sessions will be held two times a week by members of the Institute of Sport Science and Sports of the University of Erlangen-Nuremberg. Follow-up visits are scheduled three and six months after intervention period.

Enrollment

69 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Prefrailty according to the frailty score of Fried

Exclusion criteria

  • Sarcoidosis
  • Nephrolithiasis
  • Plasmacytoma
  • COPD
  • Inflammatory bowel disease
  • Rheumatoid arthritis
  • History of cancer
  • Instable heart disease
  • Depression (GDS>=6)
  • Dementia (MMSE<=24)
  • BMI>35kg/m²
  • Current attendance of muscle training
  • Medication: immunosuppressive drugs

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

69 participants in 3 patient groups

A
Experimental group
Description:
Training I
Treatment:
Procedure: Power Training
B
Experimental group
Description:
Training II
Treatment:
Procedure: Strength Training
C
Active Comparator group
Description:
Control
Treatment:
Other: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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