Pre-Active PD: Looking at Physical Activity Behavior Change in Parkinson's Disease

Parkinson Disease Clinical Trial

Official title:

Pre-Active PD: a Randomized Control Trial (RCT) Pilot Study to Improve Self-management of Physical Activity (PA) Routines in Adults With Early-stage Parkinson's Disease (PD)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05308238
• Other study ID #: MJF.AOTF.1
• Status: Active, not recruiting
• Phase: N/A
• Start date: April 18, 2022
• Est. completion date: March 2024

Study information

• Verified date: February 2024
• Source: San Jose State University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Pre-Active PD is a randomized controlled feasibility study to evaluate the implementation of a telehealth-delivered physical activity behavior change intervention for people with early-mid stage Parkinson's disease. The program utilizes occupational therapists to provide one-to-one individualized support to facilitate and optimize exercise uptake as part of their disease self-management. The structure of the intervention is based on previous research in neurodegenerative disease including Parkinson's disease and Huntington's disease.

Description:

This study will utilize a randomized controlled trial design to assess the feasibility and acceptability of the Pre-Active PD intervention for people with Parkinson's Disease who are in the early disease stage (Hoehn & Yahr stage I or II). The study will compare an experimental group (occupational therapy for exercise behavior change) to a control group (education only). Both groups will be matched for contact time. Individuals will be recruited through the Columbia University Medical Center Parkinson's Disease Center of Excellence. The study will also be listed on the Fox Trial Finder, a website maintained through the Michael J Fox Foundation. Individuals who choose to participate will be screened for eligibility using the inclusion/exclusion criteria and complete the PAR-Q+ safety screen or have medical clearance from their general practitioner. After randomization, participants will be assessed for cognition and history of occupational therapy (OT) and physical therapy (PT). Measures of acceptability will include retention and completion rates, Fitbit wear-time, and the Perceived Autonomy Support Healthcare Climate Questionnaire (PAS-HCCQ). Implementation will be assessed by the Rating Tool to Assess Fidelity of Intervention Delivery. Physical activity levels will be measured by a wearable activity monitor (Actigraph™ GT9X), worn 7 consecutive days pre and post intervention and 2nd follow-up, as well as a questionnaire. We will also use the Self-Efficacy for Exercise Scale and measure balance and mobility. Descriptive statistics (mean, standard deviation) will be calculated for all demographic information and resultant outcome measures.

Baseline and follow-up outcome measures include the following domains: exercise self-efficacy scale, exercise motivation (Behavioral Regulation In Exercise Questionnaire, physical activity levels (Brunel Lifestyle Physical Activity Questionnaire; ActiGraphTM wearable activity monitor, and Modified PA-R Question), physical performance measures (TUG Single Task and Dual Task Cognitive Version; 30 second sit-to-stand; Modified 2 Minute Step Test), self-perception measures (Modified Canadian Occupational Performance Measure; Patients' Global Impression of Change scale), and the Life Space Assessment.

Participants assigned to the occupational therapy intervention group, will receive 6 telehealth coaching sessions and 8 brief email or text check-ins over the course of 4 months. They will also receive a Fitbit and Engage PD Workbook. The third coaching session will be audio and video-recorded (if consented) and later viewed by an assessor to determine how well the intervention was delivered. The recording will be stored until completion of the study. Declining to be recorded will not affect study participation.

The OT intervention group will utilize the Pre-Active PD program (Clinicaltrials.gov NCT03696589) to guide the delivery of the intervention. This will include a checklist of the key elements that are important for the therapist in order to facilitate PA behavior change. In addition, the therapist will utilize motivational interviewing strategies that include four processes (engaging, evoking, planning, and tracking) and five core communication skills (asking open ended questions, affirming, reflective listening, summarizing, and informing and advising). The therapist will introduce the Pre-Active PD workbook and utilize it as a tool and reference for the participant in order to engage and focus them throughout the coaching process, and will educate participants on the types of exercise options and the specific exercise benefits for PD. In the planning process, the therapist will facilitate discussion on development of specific and measurable goals, and will give the participant a Fitbit physical activity monitor so that they can self-monitor their heart rate and physical activity during the course of the intervention period. The recommended exercises will be individualized to each participant but will primarily focus on increasing general physical activity (e.g. steps per day) as well as engagement in moderate-vigorous intensity aerobic exercise a minimum of three times per week. Balance and strengthening exercises will also be recommended as appropriate. Participants will also be given a short exercise safety checklist to assure safety when conducting home exercises.

Participants assigned to the disease management education group, will receive online educational videos that can be watched at their own convenience over the course of 4 months. There will be up to 6 hours of content, and the links to these online videos will be provided via email. Following completion of the study, individuals in the control group will receive an Engage PD Workbook and one OT coaching session.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 50
• Est. completion date: March 2024
• Est. primary completion date: March 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

1. Neurologist confirmed clinical dx for Parkinson's disease Hoehn & Yahr stage I or II

2. Ambulatory for indoor and outdoor mobility without assistance or assistive device

3. Successful completion of Physical Activity Readiness Questionnaire (PAR-Q), or medical clearance from GP

Exclusion Criteria:

1. Musculoskeletal injury that would prevent participation in an exercise program

2. Other neurological diseases or disorders such as stroke

3. Already engaging in aerobic exercise for at least 30 minutes for 5 or more days per week.

Related Conditions & MeSH terms

• Parkinson Disease

Intervention

Behavioral:
• Occupational therapy intervention group
Participants will receive 6 telehealth coaching sessions and 8 brief email or text check-ins over the course of 4 months. Participants will also receive a Fitbit and Engage PD Workbook.
• Disease management education group
Participants will receive online educational videos that they can watch at their own convenience over the course of 4 months. There will be up to 6 hours of content, and the links to these online videos will be provided via email. Following completion of the study, individuals in this group will receive an Engage PD Workbook and one OT coaching session, if they choose to.

Locations

Country	Name	City	State
United States	Neurorehabilitation Research Laboratory	New York	New York
United States	San Jose State Universty	San Jose	California

Sponsors (2)

Lead Sponsor	Collaborator
San Jose State University	Teachers College, Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility: Adherence	Participant completion of = 75% of sessions 1, 2 & 3	4 months
Primary	Feasibility: Retention	> 75% of all participants retained at follow-up	4 months
Primary	Change from baseline Brunel Lifestyle Physical Activity Questionnaire (Karageorghis, 2005) at 4 months and 6 months	A 10-item questionnaire that measures both pre-planned (6 items) and un-planned (3 items) lifestyle PA. Scoring for each item is on a scale of 1-5, and the scores for each subscale are averaged. Scores range from 1 (low level of physical activity) to 5 (high level of physical activity).	Baseline, 4 months, and 6 months
Primary	Change From Baseline Moderate-Vigorous Physical Activity Using Actigraph at 4 Months and 6 months	Measured using ActiGraph accelerometer, levels of moderate-vigorous physical activity will be measured, as well as number of steps and sedentary behavior.	Baseline, 4 months, and 6 months
Secondary	Change From Baseline Timed-up-and-go (TUG) at 4 Months and 6 months	Participant starts sitting in chair and then rises when prompted to "go" and then walks 3 meters, turns around, walks back to chair and sits. Time to complete is recorded. Then it is performed again with the additional element of counting backwards by 3 starting at a randomly selected number between 20 and 100.	Baseline, 4 months, and 6 months
Secondary	Change From Baseline 30 second sit-to-stand at 4 Months and 6 months	A physical performance measure which assesses functional lower extremity strength in older adults. The person is seated in a chair without arms, with feet shoulder width apart (placed on floor), and arms crossed over the chest. The participant is then encouraged to complete as many full stands as possible within 30 seconds. The number of full stands completed with the 30 sec period is the score.	Baseline, 4 months, and 6 months
Secondary	Change From Baseline Modified 2 Minute Step Test at 4 Months and 6 months	A physical performance assessment to determine a participant's cardiorespiratory fitness level. This will be completed with a caregiver (virtually trained on proper guarding) present to ensure safety.	Baseline, 4 months, and 6 months
Secondary	Change From Baseline Perceived Functional Ability (PFA) Questionnaire (George et al., 1997) at 4 Months and 6 months	2-question assessment that quantifies participants' perceived ability to complete a 1- and 3-mile distance at a comfortable pace from a scale of 1 (slow-pace) to 13 (fast pace)	Baseline, 4 months, and 6 months
Secondary	Change From Baseline Modified Canadian Occupational Performance Measure (Dedding et al., 2004) at 4 Months and 6 months	This is a questionnaire used to determine participant goals and allows participants to rate current satisfaction, importance, and performance on these goals. A scale of 1 (not satisfied at all) to 10 (extremely satisfied) is used.	Baseline, 4 months, and 6 months
Secondary	Change From Baseline Patients' Global Impression of Change scale (Hurst & Bolton, 2004) at 4 Months	Self-perception of change	Baseline, and 4 months
Secondary	Change From Baseline Life Space Assessment (Stalvey et al., 1999) at 4 Months and 6 months	Questionnaire that determines how much the person gets out and about and the spatial extent of the person's typical life space, i.e., what is the usual range of places in which the person engages in activities within the designated time frame.	0, 4 & 6 months
Secondary	Post-Intervention Acceptability Questionnaire	Structured questionnaire based on Theoretical framework of acceptability (TFA)	4 months
Secondary	Intervention Implementation	Rating Tool to Assess Fidelity of Intervention Delivery (Quinn, Trubey, et al., 2016)	4 months
Secondary	Change From Baseline Modified PA-R Questionnaire at 4 Months	1-question self-rating of physical activity level over past 6-months.	0 & 4 months
Secondary	Perceived Autonomy Support Healthcare Climate Questionnaire (HCCQ) (Williams, Freedman, & Deci, 1998):	A short questionnaire to assess intervention acceptability	4 months