MedPath

Mini-trampoline Intervention vs. Nordic Walking: Balance, Fitness and Neuropsychological Effects

Not Applicable
Completed
Conditions
Overweight
Obesity
Interventions
Other: Nordic Walking
Other: mini-trampoline
Registration Number
NCT02596152
Lead Sponsor
Arno Schmidt-Trucksäss
Brief Summary

The effects of mini-trampoline training on balance, cardiorespiratory fitness, strength and neuropsychological parameters in an overweight or obese population are unknown. The aim of this 2-arm randomized controlled trial is to compare the effects of a 12-week mini-trampoline training and a 12-week nordic walking training on balance, fitness and strength in overweight/obese individuals.

Detailed Description

A growing body of literature suggests, that obesity is not only associated with medical conditions such as diabetes, but also linked to altered gait, impaired balance and a greater likelihood of falls. Weight reduction has been shown to improve balance controle. Methods to increase physical activity are largely not accepted in this population and those which conserve the musculoskeletal system are rare. Physical activity has been shown to influence mood, quality of life and eating behavior. Mini-trampoline training has been shown to enhance stability and increase fitness.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Age 18-55 years
  • Body Mass Index ≥25 kg/m2
  • ≤ 1h regular exercise/ physical activity per week
Exclusion Criteria
  • cardiovascular or other chronic diseases not permitting sports participation
  • inability to follow the procedures of the study (e.g. due to dementia)
  • neurological disorders limiting balance or medications impairing balance
  • hypertensive blood pressure not permitting exercise (>180/100 mmHg)
  • medication: beta-blocking agents which reduce cardiac adaption abilities to exercise
  • known pregnancy with contraindications for exercise according to the guidelines of the American College of Obstetricians and Gynecologists

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nordic WalkingNordic Walkingparticipants allocated to this group will participate in a 12-week Nordic Walking group instructed training twice a week.
Mini-trampolinemini-trampolineparticipants allocated to this group will participate in a 12-week mini-trampoline group instructed training twice a week.
Primary Outcome Measures
NameTimeMethod
Postural swayassessed twice: before and after the intervention (12 weeks)

COPspeed (Center of pressure speed measured on a force plate in cm/sec) measured on a force plate in quiet stance with eyes closed

Secondary Outcome Measures
NameTimeMethod
submaximal heart rate at 50 Wattsassessed twice: before and after the intervention (12 weeks)

(HR at 50 Watts in beats/min)

maximal workassessed twice: before and after the intervention (12 weeks)

(Watts on bicycle ergometer)

motivation and barriersassessed twice: before and after the intervention (12 weeks)

(score on questionnaire)

peak oxygen uptakeassessed twice: before and after the intervention (12 weeks)

(VO2 peak in ml/kg/min)

dynamic core strengthassessed twice: before and after the intervention (12 weeks)

(Nm/kg on dynamometer)

lower body functional enduranceassessed twice: before and after the intervention (12 weeks)

(repetitions during 30-second-chair rise test)

waist circumferenceassessed twice: before and after the intervention (12 weeks)

(in cm)

cognitive flexibilityassessed twice: before and after the intervention (12 weeks)

(seconds during the Trail making test)

body muscle massassessed twice: before and after the intervention (12 weeks)

(in kg)

lower body explosive strengthassessed twice: before and after the intervention (12 weeks)

(seconds on chair rise test)

isokinetic plantar flexion strengthassessed twice: before and after the intervention (12 weeks)

(Nm/kg on dynamometer)

moodassessed twice: before and after the intervention (12 weeks)

(score on multidimensional mood questionnaire)

weight adjusted quality of lifeassessed twice: before and after the intervention (12 weeks)

(score on IWQOL questionnaire)

body dissatisfactionassessed twice: before and after the intervention (12 weeks)

(score on Figure Rating Scale)

attentionassessed twice: before and after the intervention (12 weeks)

(score on the digit span test)

functional balanceassessed twice: before and after the intervention (12 weeks)

(cm in reach test)

body fat massassessed twice: before and after the intervention (12 weeks)

(in kg)

eating behaviorassessed twice: before and after the intervention (12 weeks)

(score on FEV questionnaire)

executive planning functionassessed twice: before and after the intervention (12 weeks)

(score in the Tower of London Test (computer based version))

behavioral shift and inhibitionassessed twice: before and after the intervention (12 weeks)

(number of mistakes in the Inhib Test (computer based version))

Trial Locations

Locations (1)

University of Basel, Department of Sport, Exercise and Health

🇨🇭

Basel, Switzerland

© Copyright 2025. All Rights Reserved by MedPath