EFFECT OF COGNITIVE BEHAVIORAL THERAPY ON DEPRESSION AND QUALITY OF LIFE IN PATIENTS WITH POST COVID-19

NCT05981872 | Unknown DMC

• 1 other identifier: Rehacom on post covid
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to test the effect of Rehacom on depression and Quality of life in post covid -19 patients. The main question it aims to answer is: • Is a cognitive rehabilitation therapy will improve depression and quality of life in patients with post COVID-19? Researchers will compare Rehacom with exercise therapy to see if rehacom can improve depression and quality of life in patients with post COVID-19 neuropsychological problems.

Conditions

Post-COVID-19 Syndrome

Keywords

Rehacom; post covid-19; cognitive rehabilitation; depression; Quality of life

Outcome Measures

Primary Outcomes (3)

• The Mini- Mental State Examination (MMSE)

  The Mini- Mental State Examination (MMSE) was designed to provide a standardized, brief and practical assessment of cognitive status in geriatric patients. It is used as a brief screening tool for cognitive impairment and does not identify specific disorders. It concentrates only on the cognitive aspects of mental functions and excludes questions on mood, abnormal mental experiences as well as the form of thinking.

  The MMSE is easily administered and requires only 5-10 minutes to complete depending on the impairment of the individual

• Beck depression inventory (BDI)

  • The BDI-II contains 21 items on a 4-point scale from 0 (symptom absent) to 3 (severe symptoms). Anxiety symptoms are not assessed but affective, cognitive, somatic, and vegetative symptoms are covered, reflecting the DSM-IV criteria for major depression. Scoring is achieved by adding the highest ratings for all 21 items. The minimum score is 0 and maximum score is 63. Higher scores indicate greater symptom severity.

  easily administered and requires only 5-10 minutes to complete depending on the impairment of the individual

• .Katz Index of Independence in Activities of Daily Living

  Katz ADL is the most appropriate instrument to assess functional status as a measurement of the client's ability to perform activities of daily living independently. The Index ranks adequacy of performance in the six functions of bathing, dressing, toileting, transferring, continence, and feeding.

  easily administered and requires only 5-10 minutes to complete depending on the impairment of the individual

Study Arms (2)

post covid-19 patients with neurological symptoms as study group

EXPERIMENTAL

•Study group (A) will receive cognitive rehabilitation (Rehacom ) for 30 minutes and selected physical therapy program(that included aerobic, strength, and balance training for 30 minutes, with total duration 60 minutes. 3 sessions per week for 12 weeks.

Behavioral: rehacom

post covid-19 patients with neurological symptoms as control group

ACTIVE COMPARATOR

Control group (B) which will include 18 patients who will receive only selected physical therapy program (that included aerobic, strength, and balance training ). The treatment will conducted for 60 minutes, 3 sessions per week for 12 weeks

Behavioral: rehacom

Interventions

rehacom BEHAVIORAL

Rehacom was carried out at the cognition laboratory at Faculty of physical therapy, Cairo University for training of figural memory, attention concentration. 1. Attention concentration training consists of 24 levels of difficulties . 2. Figural memory training consists of 9 levels of difficulties. In the training session, every patient was starting training from level one and when the patient successfully finished the level, the training then Progress to the level of difficulty.

Also known as: cognitive behavioral therapy

post covid-19 patients with neurological symptoms as control group; post covid-19 patients with neurological symptoms as study group

Eligibility Criteria

• Age: 30 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• All patients will be selected according to following criteria:
• Patients from both genders (male and female).
• The age of participants ranged from 30 to 45 years .
• The patients had score more than 24 according to Mini mental state examination (MMSE).
• Patient muscle power not less than grade 3 .
• Patients are ambulant.
• Patients with confirmation of previous covid19 infection PCR TEST.
• Participants were required to live in Egypt during the pre-covid and COVID-19 pandemic.
• Patients meeting the guide line of world health organization (WHO) of long/post-covid 19 syndromes.
• Patients are "long-haulers" those who history of probable or confirmed SARS-CoV-2 infection; usually within three months from the onset of COVID-19, and last more than two months

You may not qualify if:

• The patients will be excluded if they have any of the following:
• Patient previously diagnosed with depression and currently taking medication.
• patient had prior cognitive impairment.
• Illiterate patients.
• patient had experienced another major stressful event (e.g., divorce, bereavement) in the past year.
• Checking comorbidities (sum of hypertension, diabetes, arrhythmia, myocardial infarction, Chronic Obstructive Pulmonary Disease/Asthma.
• Mild cognitive impairment, dementia, other neurodegenerative diseases, stroke, depression,
• Osteoarthritis , low back pain and prevalence of polypharmacy (5 or more drugs) at admission.

Sponsors & Collaborators

• Cairo University: lead

Study Sites (1)

Faculty of physical therapy .Cairo university

Cairo, 4240101, Egypt

Location

MeSH Terms

Conditions

Post-Acute COVID-19 Syndrome; Depression

Interventions

Cognitive Behavioral Therapy

Condition Hierarchy (Ancestors)

COVID-19; Pneumonia, Viral; Pneumonia; Respiratory Tract Infections; Infections; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases; Post-Infectious Disorders; Chronic Disease; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Behavioral Symptoms; Behavior

Intervention Hierarchy (Ancestors)

Behavior Therapy; Psychotherapy; Behavioral Disciplines and Activities

Study Officials

• Hossam M Mohammed, PHD

  Cairo University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: physical therapist

Model Details: Study group (A) which will include 18 patients who will receive cognitive rehabilitation (Rehacom ) and selected physical therapy program. Control group (B) which will include 18 patients who will receive only selected physical therapy program

Study Record Dates

• First Submitted: August 5, 2023
• First Posted: August 8, 2023
• Study Start: May 4, 2023
• Primary Completion: September 1, 2023
• Study Completion: January 1, 2024
• Last Updated: August 8, 2023

Record last verified: 2023-08

Locations

EG (1)