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Efficacy of a Recreation Therapy Wellness Recovery Program for Individuals With Parkinson's Disease

Efficacy of a Recreation Therapy Community Based Wellness Recovery Program for Individuals With Parkinson's Disease

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04164043
Enrollment
3
Registered
2019-11-15
Start date
2018-03-06
Completion date
2019-02-05
Last updated
2023-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's Disease

Keywords

Recreation Therapy, Community Based, Movement Disorder, Wellness Recovery Program

Brief summary

The Recreation Therapy Wellness Recovery Program conducts group classes which provide repetitive training of foundational skills designed specifically for those with Parkinson's Disease. The course will encourage bigger and faster movements (adapted from the Parkinson Wellness Recovery, PWR!Moves ® program) and education on optimal function.

Detailed description

The purpose of this project is to evaluate a currently active community-based Recreational Therapy (RT) Wellness Recovery Program (WRP) for individuals with Parkinson's disease (PD) to determine the efficacy of the treatment intervention. Since PD is a progressive, degenerative neurological disease, it is critical that individuals with this diagnosis remain as active as possible to slow down the progression of the disease, improve balance and strength, and increase health-related quality of life. The overall goal of this project is to determine the efficacy of a neuroplasticity physical activity program in terms of improving balance, improving health-related quality of life, reducing stress, and increasing satisfaction in exercise including social connectedness of group exercise. There is evidence that the neuroplasticity model may be a more effective type of intervention than traditional exercise programs in improving symptoms of PD. The neuroplasticity approach requires repetition of complex tasks that are high intensity and present a novel challenge. This type of intervention has been shown to improve motor and cognitive behaviors which are critical areas of decline for those with PD. The WRP program uses a comprehensive neuroplasticity-principled program that integrates exercise and wellness. The PI, Julie Bradwell, LRT/CTRS is a Certified Instructor for Parkinson Wellness Recovery Power Moves. The RT Wellness Recovery program at Wake Forest Baptist Health is modeled on the Parkinson Wellness Recovery Power Moves. Components within the program include the Parkinson Power Moves and the exercise 4 Brain Change. This study will be a 14-week study with the first two weeks of collecting baseline data and immediately following with a 12-week intervention program to increase balance, health-related quality of life, and satisfaction in exercise in individuals with PD as well as reduce stress. Most research on RT interventions for this population are in traditional settings (inpatient or rehabilitation settings). When discharged from these settings, many individuals become less active, have few social interactions and lose the benefits of exercise and physical therapy they gained while in these programs once they are home. The WRP community-based program at Wake Forest Baptist Health has the potential to prevent secondary complications as well as slow down the progression of the disease for participants. If the outcomes of this project suggest this type of intervention will improve the functional skills, quality of life, and/or satisfaction in exercise for individuals with PD and reduce stress, it will provide the RT discipline with evidenced based practice intervention for this population

Interventions

BEHAVIORALWellness Recovery Program

12-week community-based recreation therapy

Sponsors

Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

All participants will enter a 14 week baseline data collection period followed by a 12-week Wellness Recovery Program

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Potential subjects in this study will have a diagnosis of Parkinson's disease. * Potential subjects in this study are able to tolerate a 60-minute exercise program; participants complete the Parkinson Power Moves Class Application which requires a release form and a physician's signature that identifies any limitations or precautions to be taken in the program.

Exclusion criteria

* Individuals who do not have a diagnosis of Parkinson's disease or those with PD who are not medically cleared to participate in the program will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Sit to Stand TestBaseline Measure 1 performed at day 1 after signing consentMeasures functional muscle strength in the lower limbs. This test is reported in seconds.
Timed Floor Transfer TestBaseline Measure 1 performed at day 1 after signing consentMeasures vestibular balance and functional mobility to determine risk of falling. This test is reported in seconds.
Timed Up and Go (TUG) testBaseline Measure 1 performed at day 1 after signing consentTest involves a series of transitional movements including sit to stand, walking, turning and sit to stand. The test is reported in seconds.
The Blue Foam (stand) with Trek Poles TestBaseline Measure 1 performed at day 1 after signing consentTest involves lateral moves and front and back moves with or without assistance. measures level of assistance needed: supervision or modified assistance.
Parkinson's Disease Questionnaire Short Form (PDQ8)Baseline Measure 1 performed at day 1 after signing consentThis is a spcific health related quality of life instrument created for individuals with Parkinson's Disease. Likert scale (0 - 4), higher the score the greater the functioning. Overall score ranges from 0 -32. Higher scores indicate greater impact of the disease
Psychological Need Satisfaction in Exercise Scale (PNSES)Baseline Measure 1 performed at day 1 after signing consentTotal range 1-6. Lower scores denotes worse outcome.
Perceived Stress Scale (PSS-10)Baseline Measure 1 performed at day 1 after signing consentTotal range 0-4. Lower scores denotes worse/better outcome.
Pain Rating Scalecompleted week 3 after signing consent10 point rating scale, low score indicates less pain.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026