Viewing Study NCT05640167



Ignite Creation Date: 2024-05-06 @ 6:22 PM
Last Modification Date: 2024-10-26 @ 2:47 PM
Study NCT ID: NCT05640167
Status: COMPLETED
Last Update Posted: 2024-05-03
First Post: 2022-11-18

Brief Title: EMPOWER PD - Feasibility of an Interdisciplinary Clinic for People With Parkinsons Disease
Sponsor: University of Rhode Island
Organization: University of Rhode Island

Study Overview

Official Title: EMPOWER PD - Feasibility of an Interdisciplinary Clinic for People With Parkinsons Disease
Status: COMPLETED
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study is a nonrandomized pilot study of an interdisciplinary patient-centric model of health care delivery in a boot camp style structured clinic for people diagnosed with Parkinsons disease PwPD 20 participants will attend a three session EMPOWER PD clinic and a two month follow up interview The primary objective is to assess feasibility and acceptability of the newly developed clinic intervention as well as individual perception of experience and barriers
Detailed Description: This study is a nonrandomized pilot study of an interdisciplinary patient-centric model of health care delivery in a boot camp style structured clinic for people diagnosed with Parkinsons disease PwPD 20 participants will attend a three session EMPOWER PD clinic and a two month follow up interview

Participants will receive a comprehensive assessment by each member of an interdisciplinary team including physical therapy speech therapy nutrition social work or psychology and pharmacy Participants will return the following week for a half day educational symposium This is a group format and they will receive a session from each of the disciplines covering topics such as exercise nutrition communication socialization sleep hygiene medication management and coping The final clinic session will be a one hour 11 meeting where individualized recommendations will be provided A participant identified caregiver is invitedallowed to accompany the participant throughout the assessment and educational process whenever possible however no information or questionnaires are being collected from them

The primary objective is to assess feasibility and acceptability of the newly developed clinic intervention as well as individual perception of experience and barriers with data derived from a program survey and semi-structured interview completed two months after clinic completion Secondary objectives will test patient response to clinic intervention related to self-reported outcome measures SROs including Patient Centered Outcome Questionnaire PD PD Knowledge quality of life fatigue confidence with balance and self-efficacy for exercise

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None