Viewing Study NCT06587555



Ignite Creation Date: 2024-10-25 @ 7:50 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06587555
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-04

Brief Title: Correlations Between Symptoms of Anxiety Andor Depression with Dysphagia Severity Level
Sponsor: None
Organization: None

Study Overview

Official Title: Correlations Between Symptoms of Anxiety Andor Depression with Dysphagia Severity Level
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this observational study is to know any CORRELATIONS BETWEEN SYMPTOMS OF ANXIETY AND OR DEPRESSION WITH DYSPHAGIA SEVERITY LEVEL in is all of the new or ongoing patients with dysphagia in the Neurorehabilitation Department at Hasan Sadikin General Hospital Bandung and who meet the inclusion and exclusion criteria The main questions it aims to answer are

Hypothesis 1 H0 There is no correlation between increased severity of dysphagia and higher levels of anxiety symptoms H1 There is a correlation between increased severity of dysphagia and higher levels of anxiety

Hypothesis 2 H0 There is no correlation between increased severity level of dysphagia and higher level of depression symptoms H1 There is a correlation between increased severity of dysphagia and higher levels of depression

Hypothesis 3 H0 There is no correlation between increased severity level of anxiety and dysphagia and higher level of depression symptoms H1 There is a correlation between increased severity of anxiety and dysphagia and higher levels of depression
Detailed Description: This study is an analytical observational study with a cross-sectional design then correlation analysis was carried out to analyse the correlation between Severity level of dysphagia with anxiety and or depression This Study performed at Hasan Sadikin Hospital between August 2024 - March 2025

Study Subject The target population for this study is all of the new or ongoing patients with dysphagia in the Neurorehabilitation Department at Hasan Sadikin General Hospital Bandung and who meet the inclusion and exclusion criteria

Inclusion criteria

Participants aged 18 years and above
Individuals diagnosed with dysphagia by a qualified healthcare professional
Participants with documented anxiety andor depression symptoms were assessed using standardized psychological assessments
Willing to participate

Exclusion criteria

Participants who have MOCA INA 18 Participants with severe malnutrition showed by BMI WHO Asia Pacific 185 Participants with unstable hemodynamics GCS 15 Participants who had a history of diagnosed anxiety and or depression Participants who had a history of using an antipsychotic drug

Sample Size Determination

The sample size in this study was determined using correlation analysis to see the correlation between variables with a minimum number of samples of 30 research subjects obtained

Confounding Factors

1 Underlying disease
2 Age
3 Duration of Rehabilitation Therapy
4 Type of Rehabilitation Theraphy

Study Oversight

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