search
Back to results

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

Primary Purpose

Overweight, Obesity

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
mini-trampoline
Nordic Walking
Sponsored by
Arno Schmidt-Trucksäss
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Overweight focused on measuring balance, strength, barriers towards exercise, quality of life, body dissatisfaction, executive functions, eating behavior, fitness

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • University of Basel, Department of Sport, Exercise and Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mini-trampoline

Nordic Walking

Arm Description

participants allocated to this group will participate in a 12-week mini-trampoline group instructed training twice a week.

participants allocated to this group will participate in a 12-week Nordic Walking group instructed training twice a week.

Outcomes

Primary Outcome Measures

Postural sway
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

peak oxygen uptake
(VO2 peak in ml/kg/min)
submaximal heart rate at 50 Watts
(HR at 50 Watts in beats/min)
maximal work
(Watts on bicycle ergometer)
dynamic core strength
(Nm/kg on dynamometer)
lower body explosive strength
(seconds on chair rise test)
lower body functional endurance
(repetitions during 30-second-chair rise test)
isokinetic plantar flexion strength
(Nm/kg on dynamometer)
functional balance
(cm in reach test)
body fat mass
(in kg)
waist circumference
(in cm)
motivation and barriers
(score on questionnaire)
mood
(score on multidimensional mood questionnaire)
weight adjusted quality of life
(score on IWQOL questionnaire)
body dissatisfaction
(score on Figure Rating Scale)
eating behavior
(score on FEV questionnaire)
attention
(score on the digit span test)
cognitive flexibility
(seconds during the Trail making test)
executive planning function
(score in the Tower of London Test (computer based version))
behavioral shift and inhibition
(number of mistakes in the Inhib Test (computer based version))
body muscle mass
(in kg)

Full Information

First Posted
October 30, 2015
Last Updated
November 13, 2020
Sponsor
Arno Schmidt-Trucksäss
search

1. Study Identification

Unique Protocol Identification Number
NCT02596152
Brief Title
Mini-trampoline Intervention vs. Nordic Walking: Balance, Fitness and Neuropsychological Effects
Acronym
TraWaFit
Official Title
Comparison of 12-week Mini-trampoline Intervention With a Nordic Walking Intervention: Balance, Fitness and Neuropsychological Effects
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
August 2015 (Actual)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
September 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Arno Schmidt-Trucksäss

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight, Obesity
Keywords
balance, strength, barriers towards exercise, quality of life, body dissatisfaction, executive functions, eating behavior, fitness

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mini-trampoline
Arm Type
Experimental
Arm Description
participants allocated to this group will participate in a 12-week mini-trampoline group instructed training twice a week.
Arm Title
Nordic Walking
Arm Type
Active Comparator
Arm Description
participants allocated to this group will participate in a 12-week Nordic Walking group instructed training twice a week.
Intervention Type
Other
Intervention Name(s)
mini-trampoline
Intervention Description
Intervention period lasts 12 weeks, training is group instructed, twice weekly. Training sessions are one hour each. The training intensity of the two interventional arms is comparable. The training progression is defined in advance.
Intervention Type
Other
Intervention Name(s)
Nordic Walking
Intervention Description
Intervention period lasts 12 weeks, training is group instructed, twice weekly. Training sessions are one hour each. The training intensity of the two interventional arms is comparable. The training progression is defined in advance.
Primary Outcome Measure Information:
Title
Postural sway
Description
COPspeed (Center of pressure speed measured on a force plate in cm/sec) measured on a force plate in quiet stance with eyes closed
Time Frame
assessed twice: before and after the intervention (12 weeks)
Secondary Outcome Measure Information:
Title
peak oxygen uptake
Description
(VO2 peak in ml/kg/min)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
submaximal heart rate at 50 Watts
Description
(HR at 50 Watts in beats/min)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
maximal work
Description
(Watts on bicycle ergometer)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
dynamic core strength
Description
(Nm/kg on dynamometer)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
lower body explosive strength
Description
(seconds on chair rise test)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
lower body functional endurance
Description
(repetitions during 30-second-chair rise test)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
isokinetic plantar flexion strength
Description
(Nm/kg on dynamometer)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
functional balance
Description
(cm in reach test)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
body fat mass
Description
(in kg)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
waist circumference
Description
(in cm)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
motivation and barriers
Description
(score on questionnaire)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
mood
Description
(score on multidimensional mood questionnaire)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
weight adjusted quality of life
Description
(score on IWQOL questionnaire)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
body dissatisfaction
Description
(score on Figure Rating Scale)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
eating behavior
Description
(score on FEV questionnaire)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
attention
Description
(score on the digit span test)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
cognitive flexibility
Description
(seconds during the Trail making test)
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
executive planning function
Description
(score in the Tower of London Test (computer based version))
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
behavioral shift and inhibition
Description
(number of mistakes in the Inhib Test (computer based version))
Time Frame
assessed twice: before and after the intervention (12 weeks)
Title
body muscle mass
Description
(in kg)
Time Frame
assessed twice: before and after the intervention (12 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
University of Basel, Department of Sport, Exercise and Health
City
Basel
ZIP/Postal Code
4052
Country
Switzerland

12. IPD Sharing Statement

Learn more about this trial

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

We'll reach out to this number within 24 hrs