Rock Steady Boxing: A Community Based In Person Class

Sponsor
University of St. Augustine for Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05773612
Collaborator
(none)
150
1
1
37.8
4

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the feasibility and effectiveness of a non-contact Rock Steady Boxing class delivered to participants with Parkinson's Disease via an in-person community-based program. The study will also assess the overall feasibility of integrating an in-person community program within a neuromuscular course in a Doctor of Physical Therapy program.

Specific Aim: To examine the effects of an in-person community-based Rock Steady Boxing class on the functional mobility, functional endurance, cardiovascular capacity, visual-motor reaction times, quality of life, mood/affect and overall physical activity completion and fear of falling on individuals with Parkinson's Disease.

Condition or Disease Intervention/Treatment Phase
  • Other: Rock Steady Boxing Class
N/A

Detailed Description

Participants will be recruited directly from the the Brain Center (non-for-profit neurology clinic). Participants will be educated on the study but advised that their participation is voluntary and researchers will not coerce boxers to participate in the study. Once a participant agrees to participate, the Informed consent will be completed. During this time, participants will be told their participation is voluntary and they can quit at any time. he primary interventions being assessed in this study include the in-person Rock Steady Boxing Class offered at USAHS once per week. Prior to attending the Rock Steady Boxing classes, all participants must be provided with medical clearance from a referring medical doctor. The Rock Steady Boxing classes are 60-90 minutes in duration and include the following 4 components: (1) active warm up (2) functional mobility exercises (3) whole body strengthening exercises and (4) non-contact boxing exercises. During the classes, boxers' vitals are assessed using health rate monitors.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Rock Steady Boxing: A Community Based In Person Class for Patients With Parkinson Disease
Anticipated Study Start Date :
Mar 7, 2023
Anticipated Primary Completion Date :
Jan 30, 2025
Anticipated Study Completion Date :
Apr 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Other: Rock Steady Boxing classes

The Rock Steady Boxing classes are 60-90 minutes in duration twice a week and include the following 4 components: (1) active warm up (2) functional mobility exercises (3) whole body strengthening exercises and (4) non-contact boxing exercises.

Other: Rock Steady Boxing Class
Rock Steady Boxing is a non-contact fitness program designed specifically for people with Parkinson's Disease.

Outcome Measures

Primary Outcome Measures

  1. Changes over time in Activities-Specific Balance Confidence Scale (ABC) from baseline to one year [Baseline, 3 months, 6-months and 1-year post intervention]

    The ABC is a self-report measure of balance confidence in performing various activities without losing balance or experiencing a sense of unsteadiness.

  2. Changes in Falls Efficacy Scale - International from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    A self-administered questionnaire designed to assess fear of falling in mainly community-dwelling older population

  3. Changes in Parkinson's Disease Fatigue Scale from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    A patient-rated scale that measures fatigue

  4. Changes in Parkinson's Disease Questionnaire -39 from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    A 39-item self-report questionnaire, which assesses Parkinson's disease-specific health related quality over the last month.

  5. Changes in Physical Activity Scale for the Elderly (PASE) from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    The PASE measures the level of self-reported physical activity in individuals aged 65 years old or older and is comprised of items regarding occupational, household, and leisure activity during the previous 7-day period.

  6. Changes in Berg Balance Test from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    The Berg Balance Scale (BBS) is used to objectively determine a patient's ability (or inability) to safely balance during a series of predetermined tasks.

  7. Changes in 10-Meter Walk Test from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    The 10 Meter Walk Test is a performance measure used to assess walking speed in meters per second over a short distance.

  8. Changes in 6-Minute Walk Test from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance.

  9. Changes in Time Up and Go (TUG) from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    Measure of function with correlates to balance and fall risk

  10. Changes in Self-Efficacy for Exercise from baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    Self report measure of exercise self-efficacy

  11. Changes in Anticipatory & Compensatory Postural Assessment form baseline to 1-year post [Baseline, 3 months, 6-months and 1-year post intervention]

    Electromyography measure of postural stability in standing

  12. Changes in Rock Steady Boxing Questionnaire from 3-month post to 1-year post intervention [3 months, 6-months and 1-year post intervention]

    Self assessment of mobility and quality of life

  13. Changes Physical Activity Intensity Monitoring from baseline to 1-year post intervention [Baseline, 3 months, 6-months and 1-year post intervention]

    Heart rate monitoring during exercise

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Male or Female

  2. Age Range: 18 years or older

  3. History of Parkinson's Disease between Hoehn and Yarh stages I and IV

  4. Medical clearance from a referring medical doctor

  5. Able to complete all assessments

  6. Willing to complete a weekly exercise log

Exclusion Criteria:
  1. Unable to complete the assessments.

  2. Pregnant or is expected to become pregnant during study

  3. Other reasons that may limit participation in exercises. -

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of St Augustine for Health Science Miami Florida United States 33134

Sponsors and Collaborators

  • University of St. Augustine for Health Sciences

Investigators

  • Principal Investigator: Miguel Garcia, EdD, University of St Augustine for Health Science

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of St. Augustine for Health Sciences
ClinicalTrials.gov Identifier:
NCT05773612
Other Study ID Numbers:
  • PT-0401-498
First Posted:
Mar 17, 2023
Last Update Posted:
Mar 17, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2023