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CompletedNCT01014663Updated Apr 2, 2020

Non-contact Boxing Training and Traditional Therapeutic Exercise for Persons With Parkinson's Disease

An interventional study of Traditional Therapeutic Exercise and Non-Contact Boxing Training in Parkinson's Disease, sponsored by University of Indianapolis. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-04-02.

Sponsored by University of Indianapolis · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The primary purpose of this study is to compare the effects of a non-traditional boxing training program to a traditional therapeutic exercise program on activity and participation outcomes in persons with Parkinson's disease. Thirty participants will be randomly assigned to participate in either non-contact boxing training or traditional therapeutic exercise for 36 sessions over 12 weeks. Participants will be measured immediately before (pre-test) and after (post-test) the intervention.

Read the detailed description

Physical therapists commonly treat patients with Parkinson's disease. Typical clinical interventions used by physical therapists including strengthening, stretching and aerobic training have been shown to improve function and quality of life of persons with Parkinson's disease. Alternative exercise interventions that incorporate non-traditional concepts, such as tango dance, tai chi and taiji have also been found to lead to improvements in function in persons with Parkinson's disease. It is important that comparisons between different types of exercise programs for persons with Parkinson's disease be explored in order to determine effective options for care.

Here in Indianapolis, Indiana, individuals with Parkinson's disease have a unique opportunity for alternative exercise with the recent development of the popular non-contact boxing training program offered by the Rock Steady Boxing Foundation. Therefore, the purpose of this study is to compare the effects of the non-traditional boxing training program to a traditional therapeutic exercise program on activity and participation outcomes in persons with Parkinson's disease.

Thirty participants with Parkinson's disease will be recruited from Central Indiana. All potential participants will be screened to determine eligibility for the study. Participants who are eligible and give consent will be randomly assigned to participate in either the non-contact boxing training or the traditional therapeutic exercise program for 36 sessions lasting over 12 weeks with 60-90 minutes of exercise each session. Participants will be measured immediately before (pre-test) and after (post-test) the intervention period.

02

Conditions studied

  • Parkinson's Disease

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Keywords

  • Parkinson's disease
  • exercise
  • training program
  • rehabilitation
  • boxing
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • diagnosis of Parkinson's disease
  • currently not receiving physical therapy services
  • medically stable with a physician release stating approval to enter an exercise program
  • independently ambulatory in the home setting with or without the use of an assistive device
  • able to follow at least three step verbal commands
  • available for the entire period of the study
  • have transportation to and from training and measurement sessions

Exclusion criteria

Exclusion Criteria:

  • preexisting neurological conditions other than Parkinson's disease
  • current musculoskeletal conditions that would limit participation in either training program
  • significant orthopedic surgery within the past six months
  • past brain surgery or brain stimulator implant
  • currently known pregnant
  • pre-existing cardiovascular conditioner that would prohibit participation in an exercise program
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
31 participants (actual)

Study arms

  • Active comparator
    Therapeutic Exercise

    Behavioral: Traditional Therapeutic Exercise

  • Active comparator
    Non-Contact Boxing Training

    Behavioral: Non-Contact Boxing Training

Interventions

  • BehavioralTraditional Therapeutic Exercise

    The therapeutic exercise program will consist of warm-up and stretching, seated and standing range of motion activities, endurance and resistance training, balance training and a cool down. Training will take place for 36 sessions, three times/week for 60-90 minutes per session.

  • BehavioralNon-Contact Boxing Training

    Non-contact boxing training will consist of warm-up and stretching, non-contact boxing training (including punching a focus mitt, speed and heavy punching bags), endurance training activities, strength and resistance training, and a cool down. Training will take place for 36 sessions, three times/week for 60-90 minutes per session.

05

What researchers measure

Primary outcomes

  1. Mobility: Measured with the Timed Up and Go Test; Four-Square Step Test; Six-Minute Walk Test; Berg Balance Scale; Functional Reach Test

    Time frame: Each outcome measures is assessed at pre-test (immediately before intervention), post-test (immediately after the 12 week intervention).

Secondary outcomes

  1. Participation: measured with the Activities Specific Balance Confidence Scale and the Parkinson's disease Quality of Life Scale

    Time frame: Each outcome measures is assessed at pre-test (immediately before intervention), post-test (immediately after the 12 week intervention).

06

Study locations

1 site
  • University of Indianapolis, Krannert School of Physical Therapy
    Indianapolis, Indiana 46227, United States
07

Registry details

Key details

Study ID
NCT01014663
Lead sponsor
University of Indianapolis
Responsible party
Stephanie Miller (Associate Professor, University of Indianapolis) — Principal investigator
First posted
Nov 17, 2009
Start date
Sep 2009
Primary completion
Dec 2010
Completion
Mar 2011
Last update
Apr 2, 2020

Study contacts

Stephanie A Combs, PT, PhD, NCS
principal investigator · University of Indianapolis
Dyer M Diehl, PT, PhD
principal investigator · University of Indianapolis
William H Staples, PT, DPT, GCS
principal investigator · University of Indianapolis

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.

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