Effects Resistance Training on Motor Control and Cognition (KFPS_2)

February 6, 2018 updated by: University of Kassel

Effects of Different Resistance Training Methods on Strength, Motor Control and Executive Functions in Older Adults

It is well documented that both balance and resistance training have the potential to mitigate intrinsic fall risk factors in older adults. Recently, it was shown that a simultaneously executed balance and resistance training, namely resistance training on uneven surfaces is an eligible, effective and safe alternative training program to mitigate intrinsic fall risk factors in older adults. However, knowledge about the effects of specific adductor and abductor training has advantages over traditional resistance training and resistance training on unstable surfaces regarding forward propulsion. Further, the effects of different kinds of resistance training on cognition, especially embodiment is investigated.

Study Overview

Detailed Description

Introduction: In the course of ageing, physical abilities decline and consequently there is an increase in risk of falling and fall incidences. Notwithstanding, the fact that causes of falls are multifactorial, losses in lower-extremity muscle strength, power and balance seem to be the most prominent intrinsic (i.e., person-related) fall risk factors in older adults. Several systematic reviews and meta-analyses highlighted the positive effects of resistance and balance training when applied as a single means, on measures of leg muscle strength, power and balance in older adults. Recently, it was shown that a simultaneously executed balance and resistance training, namely resistance training on uneven surfaces is an eligible, effective and safe alternative training program to mitigate intrinsic fall risk factors in older adults. Based on several investigations, it can be safely assumed that exercises conducted on unstable devices activate smaller muscles and stabilising function of bigger muscle groups. This facilitates torque and power transfer from lower to upper extremeties and is possibly responsible for similar effects as compared to stable resistance training despite lower loads. However, it is unknown if resistance training targeting adductor and abductor muscles induces similar results as compared to resistance training conducted on uneven surfaces. Moreover, physical activity has proven to affect cognitive measures positively, especially executive functions. It has yet to be determined to what extent different kinds of resistance training affect executive functions.

Methods/Design: This study is a three-arm, 10-week RCT with a 10-week no-contact follow-up. Participants were randomly allocated (1:1) to either: 1) machine-based stable resistance training (M-SRT); 2) free-weight unstable resistance training (F-URT); 3) machine-based adductor and abductor resistance training. The design and reporting of this study follows the CONSORT (Consolidated Standards of Reporting Trials) 2010 Statement for parallel group randomised trials.

Setting Participants are recruited from the communities in and around Kassel, Germany. Screening visits, measurement sessions, and the interventions are held at the Insitute of Sports and Sports Science / University of Kassel, Germany.

Recruitment strategies: Recruitment is carried out by placing 1) an advertisement in the local newspaper, 2) during a public information meeting at the local town hall and 3) word of mouth. Interested individuals contact the study coordinator by phone, where they are provided with a brief description of the study. If responses suggest study eligibility then interested individuals are invited to attend a formal in-person screening visit.

Participants:Older adults are eligible if they: 1) are aged between 65 and 80 years old 2) and able to walk independently for more than 10m. An a priori power analysis using G*Power 3.1 with an assumed type I error of .05 and a type II error of .10 (90% statistical power, correlation among groups: .5, nonsphericity correction: 1) was computed to determine an appropriate sample size to detect medium (.50 ≤ d ≤ .79) interaction effects. The calculations were based on a study assessing the effects of core strength training using unstable devices on older adults. The analysis revealed the requirement of 54 participants (18 per group) to obtain medium "time x group" interaction effects. Considering the likelihood of dropouts, at least 83 participants are going to be recruited to compensate for a possible dropout rate of ~20%.

Interventions: All intervention groups train for ten weeks, twice per week on non-consecutive days for 60 minutes each. The 10-week intervention period consistes of a one week introductory phase and three major training blocks lasting three weeks each. Training intensity is progressively and individually increased over the 10-week training program by modulating load and sets for all groups and level of instability for F-URT. After week one (50 %), four (60%), and seven (70%) the training load (weight) is increased following one repetition maximum (1-RM) testing for each major exercise. M-SRT followes a 'traditional' machine-based stable resistance training program, including squats with a smith-machine and a leg press. F-URT conducts squats and front lunges on unstable devices. M-ART uses adductor and abductor strength training machines. All three intervention groups conduct a resistance training program consisting of two main exercises, a preparation and cool-down phase. Participants perform ten minutes of low-intensity stepping on a stair-walker as a brief warm-up at the beginning of each training session, followed by the resistance exercises and walking on a treadmill as cool-down. Training under unstable surface conditions, especially with additional weight, implies a certain degree of accident risk. Due to this factor, all instability exercises are observed by instructors and secured with additional aids like boxes. Training is supervised by skilled instructors at all times. For the first two weeks the participant to instructor ratio will be 5:1, thereafter 10:1.

Outcome assessment: Outcomes are measured at baseline, 10 weeks (intervention endpoint) and 20 weeks (study endpoint). Measurement sessions are conducted on one day.

Baseline data: Baseline measurements are obtained prior to randomisation. In addition to the measurements described below, the following are also collected: demographic and general health characteristics; medical history and medications; anthropometrics and rate of falls / near falls.

Study Type

Interventional

Enrollment (Actual)

82

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years to 80 years (Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • between 65 and 80 years old
  • ability to walk independently without any gait aid

Exclusion Criteria:

  • pathological ratings of the Clock Drawing Test (CDT),
  • Mini-Mental-State-Examination (MMSE, < 24 points),
  • Falls Efficacy Scale - International (FES-I, > 24 points),
  • Geriatric Depression Scale (GDS, > 9 points),
  • Freiburg Questionnaire of Physical Activity (FQoPA, < 1hour)
  • Frontal Assessment Battery (FAB-D, < 18 points)
  • any neurological, musculoskeletal or heart-related disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: M-SRT
Machine-based stable resistance training. Exercising 'traditional' machine-based resistance training.
traditional machine-based resistance training
Experimental: F-URT
Free weight unstable resistance training; conducted free-weight resistance training on unstable devices using dumbbells instead of exercise-machines.
free weight resistance training using unstable devices
Experimental: M-ART
Machine-based adductor/abductor resistance training. Exercising with 'traditional' adductor/abductor machines.
machine-based adductor/abductor resistance training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical Gait Analysis
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
changes in variance components (Vucm, Vort, Vtot) of an uncontrolled manifold analysis; measured in rad²
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximal isometric leg extension strength (ILES)
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in isometric strength, measured in N
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Fall self-efficacy Questionnaire
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in anxiety score
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Proactivec Balance (timed up and go test)
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in leg strength and procative balance (seconds)
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Power tests (chair rise test)
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in muscle power (seconds)
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Maximal isometric adductor and abductor strength
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in isometric strength, measured in N
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Stroop Task
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in reaction time to congruent and incongruent stimuli (ms)
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
Proactivec Balance (multidirectional reach test)
Time Frame: Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)
change in proactive balance (cm)
Pre test -> Intervention (10 weeks) -> Post test (within 2-5 days after the intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Armin Kibele, PhD, University of Kassel

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2017

Primary Completion (Actual)

April 1, 2017

Study Completion (Actual)

April 1, 2017

Study Registration Dates

First Submitted

January 4, 2017

First Submitted That Met QC Criteria

January 9, 2017

First Posted (Estimate)

January 11, 2017

Study Record Updates

Last Update Posted (Actual)

February 7, 2018

Last Update Submitted That Met QC Criteria

February 6, 2018

Last Verified

February 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Raw results will be published. Age will be described as intervals (65-69, 70-74, 75-80) and height will be removed, thus no backtracking is possible

IPD Sharing Time Frame

when the article is published

IPD Sharing Access Criteria

IPD will be published as supplementary material. Raw results will be published. Age will be described as intervals (65-69, 70-74, 75-80) and height will be removed, thus no backtracking is possible

IPD Sharing Supporting Information Type

  • SAP

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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