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KEEP Intervention for People Newly Diagnosed With Parkinson's (KEEP)

Primary Purpose

Parkinson Disease

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
KEEP Intervention
control
Sponsored by
University of Cambridge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Parkinson Disease focused on measuring Physical activity, education, exercise, self-efficacy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of Idiopathic Parkinson's Disease
  • Within 12 months since diagnosis
  • Stable medication regime for four weeks prior to initiation of trial
  • Ability to understand written English

Exclusion Criteria:

  • Acute illness
  • History of neurological disorder other than Parkinson Disease
  • Diagnosis of dementia or significant cognitive impairments
  • Participation in NHS structured PD-specific education program with or without exercise classes in the last year
  • Unable to understand written English

Sites / Locations

  • Department of Psychiatry

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention group

Control Group

Arm Description

The experimental group will receive: Online education modules Online group discussions facilitated by Specialist Physiotherapist

The comparator for this study is usual care pathway. Under the usual care pathway, participants will receive education booklets on exercise by Parkinson's UK.

Outcomes

Primary Outcome Measures

Acceptability assessment 1: Recruitment rate
Assessment of recruitment rate of study (% of eligible participants enrolled)
Acceptability assessment 2: Education programme compliance
Compliance with the online education programme (% of sessions completed)
Acceptability assessment 3: Drop out rate
Comparison of drop out rates (%) between the intervention group and control group
Acceptability assessment 4: Acceptability of Intervention
A questionnaire designed to assess satisfaction with the education intervention. it includes multiple choice and open ended questions.
Feasibility of delivering the intervention online
Assessment of any technical problems or difficulties accessing online intervention as reported by participants

Secondary Outcome Measures

Unified Parkinson's Disease Rating Scale Part 3
The UPDRS is the gold-standard scale for Parkinson's assessment and has four parts. For this study only UPDRS III, motor examination will be completed by a trained assessor. UPDRS III total scores range from 7 to 86 points, with higher scores indicating more severe impairment..
MiniBESTest
The Mini-BEST is a 14-item scale that assesses dynamic balance components including anticipatory postural adjustments, reactive postural control, sensory orientation and dynamic gait. The data is based on a total score of 28 points, with higher score indicating better task performance.
Five time Sit To Stand
Five time sit to stand is a validated test used to assess functional lower extremity strength, balance and risk falls in older adults. It has been used in PD population with high interrater and test-retest reliability. Longer time to complete indicates worse task performance.
Self-efficacy for Exercise
The Self-Efficacy for exercise (SEE) scale is a 9-item validated scale which assesses a person self-efficacy to exercise under different circumstances. This scale is a modified version of Bandura's Exercise Self-Efficacy Scale and ask participants to rate their perceived exercise efficacy on a scale form 0 meaning not confident at all to 10 meaning very confident. Higher score indicate higher self-efficacy
Hospital Anxiety and Depression Scale
Hospital Anxiety and Depression Scale (HADS) is a widely used questionnaire to measure anxiety and depression. A self-reported brief instrument which includes 14 questions aiming to detect and indicate severity of anxiety and depression. It has been used before and is a validated and reliable tool to use in Parkinson's population.
Apathy Evaluation Scale
Apathy Evaluation Scale (AES) is a standardised and validated self-rating instrument to evaluate apathy. It consists of 18 items that are scored on a 4-point Likert Scale, with highest score indicating more severe apathy
Multidimensional Outcome Expectation Scale
Outcome expectations about the benefits of regular exercise and PA will be measured by the Multidimensional Outcomes Expectations for Exercise Scale (MOEES). The MOEES has 15 items that reflect three subdomains of outcome expectations. The items were rated on a five-point scale from 1 (Strongly disagree) to 5 (Strongly agree) and summed to form the subscale measures of outcome expectations with higher scores reflecting greater beliefs about the benefits of regular exercise and physical activity.
Oxford Participation and Activities Questionnaire
Oxford Participation and Activities Questionnaire (Ox-PAQ) is a patient-reported outcome measure comprised of 23 items aiming to assess participation and activity in patients with long-term conditions.
Recent Physical Activity Questionnaire
Physical Activity will be measured subjectively and objectively. Subjectively it will be measured via the self-reported Recent Physical Activity Questionnaire (RPAQ), which is designed to assess PA in everyday life in the last 4 weeks. The questionnaire has three sections assessing a range of activities in different domains (around the house, work and recreation).
Knowledge of Exercise and Physical Activity
Knowledge of Exercise and Physical Activity questionnaire is a 10-item knowledge questionnaire around the role of exercise and physical activity in the management of PD and it has been designed by the PI to assess knowledge levels. A total score of 10 indicates better knowledge scores.
Wrist-worn accelerometer
Objectively, physical activity will be measured with the use of a wrist-worn accelerometer (GeneActiv monitor) over 7 consecutive days.

Full Information

First Posted
February 2, 2022
Last Updated
November 1, 2022
Sponsor
University of Cambridge
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1. Study Identification

Unique Protocol Identification Number
NCT05253040
Brief Title
KEEP Intervention for People Newly Diagnosed With Parkinson's
Acronym
KEEP
Official Title
KEEP- A Randomised Feasibility Study of a Co-designed Physical Health Education Intervention to Improve Knowledge, Exercise Efficacy and Participation for Newly Diagnosed People With Parkinson's.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 18, 2022 (Actual)
Primary Completion Date
September 21, 2022 (Actual)
Study Completion Date
June 18, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cambridge

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Parkinson's Disease (PD) is a progressive neurological condition that affects movement, balance and cognition, resulting in loss of independence and compromised quality of life over the course of the condition. Research suggests that those detrimental outcomes can be reduced through physical activity (PA) and exercise, especially when those are started early. Educating people with Parkinson's (PwP) on the role of PA and exercise in PD progression can boost PA engagement by increasing enablers such as exercise self-efficacy and removing barriers such as misinformation about exercise and exercise outcomes. Working closely with PwP and healthcare professionals, a physical health education programme was co-designed to address the needs and preferences of PwP around exercise and PA education. The process was supervised by the patient and Public Involvement group attended by PwP, academics, researchers and clinicians working with PwP. The study will utilise an assessor blinded randomised controlled design to investigate the acceptability and feasibility of delivering an online physical health education programme for PwP who are newly diagnosed. Thirty PwP, diagnosed in the last 12-months, will be randomly allocated into two groups: 1) the intervention group in which participants will receive online education modules and will be invited to attend virtual group sessions with a specialist neuro-physiotherapist; 2) the control group which will follow the usual care pathway and participants will receive Parkinson's UK booklets. The aim of the study is to explore an alternative approach to standard care regarding patient education in PD and evaluate the feasibility and acceptability of a co-designed education intervention for newly diagnosed PwP delivered online. Feasibility data will be collected during the study and acceptability data will be assessed via a questionnaire at the end. Outcomes including PA levels, exercise knowledge, exercise efficacy, and participation will be assessed at baseline, post-intervention and at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Physical activity, education, exercise, self-efficacy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
The experimental group will receive: Online education modules Online group discussions facilitated by Specialist Physiotherapist
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
The comparator for this study is usual care pathway. Under the usual care pathway, participants will receive education booklets on exercise by Parkinson's UK.
Intervention Type
Other
Intervention Name(s)
KEEP Intervention
Intervention Description
Educational intervention
Intervention Type
Other
Intervention Name(s)
control
Intervention Description
booklet from Parkinson's UK
Primary Outcome Measure Information:
Title
Acceptability assessment 1: Recruitment rate
Description
Assessment of recruitment rate of study (% of eligible participants enrolled)
Time Frame
Through study completion (12 months)
Title
Acceptability assessment 2: Education programme compliance
Description
Compliance with the online education programme (% of sessions completed)
Time Frame
Through study completion (12 months)
Title
Acceptability assessment 3: Drop out rate
Description
Comparison of drop out rates (%) between the intervention group and control group
Time Frame
Through study completion (12 months)
Title
Acceptability assessment 4: Acceptability of Intervention
Description
A questionnaire designed to assess satisfaction with the education intervention. it includes multiple choice and open ended questions.
Time Frame
Completed at the end of participation in the study (after 8 weeks)
Title
Feasibility of delivering the intervention online
Description
Assessment of any technical problems or difficulties accessing online intervention as reported by participants
Time Frame
Through study completion (12 months)
Secondary Outcome Measure Information:
Title
Unified Parkinson's Disease Rating Scale Part 3
Description
The UPDRS is the gold-standard scale for Parkinson's assessment and has four parts. For this study only UPDRS III, motor examination will be completed by a trained assessor. UPDRS III total scores range from 7 to 86 points, with higher scores indicating more severe impairment..
Time Frame
Baseline(week 0) and follow up (6-month post intervention)
Title
MiniBESTest
Description
The Mini-BEST is a 14-item scale that assesses dynamic balance components including anticipatory postural adjustments, reactive postural control, sensory orientation and dynamic gait. The data is based on a total score of 28 points, with higher score indicating better task performance.
Time Frame
Baseline(week 0) and follow up (6-month post intervention)
Title
Five time Sit To Stand
Description
Five time sit to stand is a validated test used to assess functional lower extremity strength, balance and risk falls in older adults. It has been used in PD population with high interrater and test-retest reliability. Longer time to complete indicates worse task performance.
Time Frame
Baseline(week 0) and follow up (6-month post intervention)
Title
Self-efficacy for Exercise
Description
The Self-Efficacy for exercise (SEE) scale is a 9-item validated scale which assesses a person self-efficacy to exercise under different circumstances. This scale is a modified version of Bandura's Exercise Self-Efficacy Scale and ask participants to rate their perceived exercise efficacy on a scale form 0 meaning not confident at all to 10 meaning very confident. Higher score indicate higher self-efficacy
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Hospital Anxiety and Depression Scale
Description
Hospital Anxiety and Depression Scale (HADS) is a widely used questionnaire to measure anxiety and depression. A self-reported brief instrument which includes 14 questions aiming to detect and indicate severity of anxiety and depression. It has been used before and is a validated and reliable tool to use in Parkinson's population.
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Apathy Evaluation Scale
Description
Apathy Evaluation Scale (AES) is a standardised and validated self-rating instrument to evaluate apathy. It consists of 18 items that are scored on a 4-point Likert Scale, with highest score indicating more severe apathy
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Multidimensional Outcome Expectation Scale
Description
Outcome expectations about the benefits of regular exercise and PA will be measured by the Multidimensional Outcomes Expectations for Exercise Scale (MOEES). The MOEES has 15 items that reflect three subdomains of outcome expectations. The items were rated on a five-point scale from 1 (Strongly disagree) to 5 (Strongly agree) and summed to form the subscale measures of outcome expectations with higher scores reflecting greater beliefs about the benefits of regular exercise and physical activity.
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Oxford Participation and Activities Questionnaire
Description
Oxford Participation and Activities Questionnaire (Ox-PAQ) is a patient-reported outcome measure comprised of 23 items aiming to assess participation and activity in patients with long-term conditions.
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Recent Physical Activity Questionnaire
Description
Physical Activity will be measured subjectively and objectively. Subjectively it will be measured via the self-reported Recent Physical Activity Questionnaire (RPAQ), which is designed to assess PA in everyday life in the last 4 weeks. The questionnaire has three sections assessing a range of activities in different domains (around the house, work and recreation).
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Knowledge of Exercise and Physical Activity
Description
Knowledge of Exercise and Physical Activity questionnaire is a 10-item knowledge questionnaire around the role of exercise and physical activity in the management of PD and it has been designed by the PI to assess knowledge levels. A total score of 10 indicates better knowledge scores.
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)
Title
Wrist-worn accelerometer
Description
Objectively, physical activity will be measured with the use of a wrist-worn accelerometer (GeneActiv monitor) over 7 consecutive days.
Time Frame
Baseline(week 0), post intervention (week 8) and follow up (6-month post intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of Idiopathic Parkinson's Disease Within 12 months since diagnosis Stable medication regime for four weeks prior to initiation of trial Ability to understand written English Exclusion Criteria: Acute illness History of neurological disorder other than Parkinson Disease Diagnosis of dementia or significant cognitive impairments Participation in NHS structured PD-specific education program with or without exercise classes in the last year Unable to understand written English
Facility Information:
Facility Name
Department of Psychiatry
City
Cambridge
ZIP/Postal Code
CB2 0SZ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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KEEP Intervention for People Newly Diagnosed With Parkinson's

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