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Effect of Eight-week Concurrent Training on Functional Capacity in Patients With Unilateral Transtibial Amputation

U

University of Sao Paulo General Hospital

Status

Completed

Conditions

Sequelae
Amputation of Lower Limb Above Knee

Treatments

Other: Concurrent Training

Study type

Interventional

Funder types

Other

Identifiers

NCT04165434
Amputados

Details and patient eligibility

About

OBJECTIVES: To assess the effect of concurrent training (CT) of an eight-week on strength, power and cardiorespiratory fitness on muscle condition, balance, load distribution in the lower limbs and aerobic capacity in patients with unilateral transtibial amputation (UTA). MATERIAL AND METHODS: Twenty-six individuals with prosthesis over 3-months were selected. Patients were randomly divided into two groups. Group 1 (n = 17) denominated UTA who performed the evaluation and training recommended by the prosthesis (bodybuilding vs. aerobic interval-training on the exercise cycle ergometer). Group 2 (n = 9) denominated untrained unilateral transtibial (UUT) amputees who after the evaluation were not included for the recommended training. All patients were evaluated at the baseline time of randomization and eight weeks after

Full description

OBJECTIVES: To assess the effect of concurrent training (CT) of an eight-week on strength, power and cardiorespiratory fitness on muscle condition, balance, load distribution in the lower limbs and aerobic capacity in patients with unilateral transtibial amputation (UTA). MATERIAL AND METHODS: Twenty-six individuals with prosthesis over 3-months were selected. Patients were randomly divided into two groups. Group 1 (n = 17) denominated UTA who performed the evaluation and training recommended by the prosthesis (bodybuilding vs. aerobic interval-training on the exercise cycle ergometer). Group 2 (n = 9) denominated untrained unilateral transtibial (UUT) amputees who after the evaluation were not included for the recommended training. All patients were evaluated at the baseline time of randomization and eight weeks after. The evaluation consisted of anamnesis (inclusion criteria), clinical and functional evaluation, cardiopulmonary exercise testing, isokinetic knee testing, static and dynamic posturography. The age of the group was 28.5 ± 7.1 years old, BMI 25 ± 4.8 kg.m-2, amputation time 22 ± 27.5 months, 83% were men and 57% with amputation on the left side, 11% used antidepressants and 11% antihypertensive medicine.

KEYWORDS: Transtibial amputation; Concurrent training; Rehabilitation, Comparative Study.

Enrollment

26 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • Transtibial amputation (any etiology)
  • Age between 18 - 50 years
  • Absence of any musculoskeletal and/or inflammatory diseases; central and/or peripheral neuropathy; psychiatry alteration
  • Discharge of the rehabilitation program and the use of a prosthesis for three or more months and more.

Exclusion criteria

  • Pain or inability to complete any of the tests
  • High blood pressure (over 130 x 90 mmHg) before strength evaluation
  • Loss of three consecutive training sessions and no return for the reevaluation session

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups

Experimental
Experimental group
Description:
Untrained unilateral transtibial amputees who underwent the assessment and recommended training.
Treatment:
Other: Concurrent Training
Control
No Intervention group
Description:
Untrained unilateral transtibial amputees who after the evaluation were not included for the recommended training.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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