Viewing Study NCT06370390



Ignite Creation Date: 2024-05-06 @ 8:25 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06370390
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-17
First Post: 2024-04-13

Brief Title: Community-based Group Rehabilitation Program for Stroke Patients With Dysphagia
Sponsor: Copka Sonpashan
Organization: Chao Phya Abhaibhubejhr Hospital

Study Overview

Official Title: Community-based Group Rehabilitation Program for Stroke Patients With Dysphagia a Randomized Controlled Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
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: Community-based exercise programs have demonstrated potential for implementation in older adults however it remains imperative to ascertain whether this strategy will yield comparable benefit in stroke patients with dysphagiaParticipants were randomly assigned to either the intervention group or the control group Patients in the intervention group received swallowing function training in community public spaces for 5 days every week for four-week period 60 minutes per day Patients in the control group received no intervention Penetration-Aspiration Scale and Standardized Swallowing Assessment SSA depressive symptoms Geriatric Depression Scale-15 and meal duration were assessed before and after all the treatment
Detailed Description: Stroke is complicated by oropharyngeal dysphagia in 29 to 81 of patients Up to 40 of these individuals continue to experience swallowing difficulty even after a year later which is associated with an increased risk of consequences such as aspiration pneumonia dehydration and malnutrition

Community-based exercise programs have demonstrated potential for implementation in older adults however it remains imperative to ascertain whether this strategy will yield comparable benefit in stroke patients with dysphagiaParticipants were randomly assigned to either the intervention group or the control group Patients in the intervention group received swallowing function training in community public spaces for 5 days every week for four-week period 60 minutes per day Patients in the control group received no intervention Penetration-Aspiration Scale and Standardized Swallowing Assessment SSA depressive symptoms Geriatric Depression Scale-15 and meal duration were assessed before and after all the treatment

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