Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06587555

Correlations Between Symptoms of Anxiety And/or Depression with Dysphagia Severity Level

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
Universitas Padjadjaran · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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 and/or 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 \< 18.5 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

Conditions

Timeline

Start date
2024-10-01
Primary completion
2025-02-01
Completion
2025-03-01
First posted
2024-09-19
Last updated
2024-09-19

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT06587555. Inclusion in this directory is not an endorsement.