Status
Conditions
Treatments
About
There is a rising concern about quality of life of multiple sclerosis (MS) patients has emerged. Cognitive dysfunction with primary fatigue and there correlation to the level of disease inflammatory process has got great interest in MS research .
The aim of the present study was to examine the influence of using a computer-based cognitive behavioral therapy on primary fatigue, cognitive dysfunction, and inflammatory biomarkers for patients with MS.
Patients and methods A total of 40 MS patients (Expanded Disability Status Scale<5) were divided into two groups, both groups are suffering cognitive decline (using RehaCom software to assess attention/concentration, memory and reaction behavior) with primary fatigue according to the Fatigue Severity Scale (FSS>36). Patients with depression and sleep problems were excluded from the study. Patients in both groups have elevated serum levels of tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ).
Patients in (G1) underwent conventional physical therapy program for MS including aerobic training, resistive training and a flexibility program, patients in (G2) underwent an intensive computer-based cognitive program for attention, concentration, memory and reaction behavior using the RehaCom software.
The conventional physical therapy interventions for both (G1) sustained for three months, 45 minutes to 1 hour, 3 times/week. The computer-based cognitive behavioral therapy for patients in (G2) was prescribed as following (45 minutes to 1 hour a session, 3 times/week for continues three months).
Full description
This study was done to to examine the influence of using a computer-based cognitive behavioral therapy on primary fatigue, cognitive dysfunction, and inflammatory biomarkers for patients with MS. This study was conducted in the time period between December 2020 till May 2021.
Subjects Selection:
Forty MS patients were selected from Neurology Department Faculty of Medicine, Cairo University out-patient clinic , Multiple Sclerosis Research Unit, Cairo University and from Faculty of Physical Therapy ,Cairo University out-patient clinic. The patients were diagnosed and referred from a neurologist. All the patients were referred from a neurologist as a clinically definite MS according to Mcdonald criteria. The diagnosis was confirmed by MRI. The patients were assigned into two equal groups (Conventional physical therapy program)(G1) & ( Computer-based cognitive behavioral therapy)(G2).
Inclusion criteria:
Exclusion criteria:
The patients were excluded when they met one of the following criteria:
Instrumentations & Procedures :
A. Assessment Interventions:
• Fatigue severity scale (FSS) : It is valid and reliable scale used to assess fatigue severity in MS patients , and to distinguish fatigued MS patients from non fatigued MS patients(Armutlu et al,2007). It is self reported questionnaire consisted of nine sentences. A list of statements/questions is provided. These statements are related to the different aspects of fatigue and how it affects the body.
Expanded Disability Status Scale (EDSS)was used to exclude patients with fatigue secondary to moderate to severe disability. It provides a total score on a scale that ranges from zero to ten. The first levels 1.0 to 4.5 indicate people with a high degree of ambulatory ability. The subsequent levels 5.0 to 9.5 indicate loss of ambulatory ability. Grade (Zero) indicate normal neurologic exam. Grade (Five) indicate the ability of the patient to ambulate without aid or rest for 200 meter but disability is severe enough to impair full daily activities. (Ten) indicate death due to MS.
Beck depression inventory scale (BDI) was used to exclude patients suffering from fatigue secondary to depression. It composed of twenty one questions each with four possible responses ranging from "zero to three". Each question assess a specific symptom common among people with depression.
Epworth Sleepiness Scale (ESS)was used to exclude the patients suffering from fatigue secondary to sleep disturbance. It assess daytime sleepiness in people with multiple sclerosis . It consists of eight questions regarding sleep in different physiological and psychological conditions in multiple sclerosis patients.
Rehacom Software to assess cognitive function : It is a computer-based intensive cognitive rehabilitation test used to assess patient's cognitive functions. It includes 32 assessment tasks for attention, memory , logical reasoning& executive functioning. It composes of regular PC , 1G RAM , DVD drive, 100 GB hard drive with windows XP SP3, 128 MB RAM direct 3D graphic card , Screen at least 19" , regular PC keyboard or Rehacom panel & printer .The Rehacom software version is (patient enpult (1990-1997) EN/ISO-13485-certified). It is characterized by easy handling, close to reality , motivating for patients.
Blood analysis: A blood sample was collected from each patient in both groups before and after the 4 months treatment intervention. Assessment of patients on immunomodulatory therapy was postponed 36 hours from the last dose. Serum blood samples were immediately stored on ice. TNF-α and IFN- γ were measured using The Quantikine Human TNF-alpha & IFN-gamma Immunoassay ELISA kit . It is a 3.5 or 4.5 hour solid phase ELISA designed to measure human TNF-alpha & IFN-gamma in cell culture supernates, serum, and plasma. It contains E. coli-derived recombinant human TNF-alpha, IFN-gamma and antibodies raised against this protein and antibodies raised against the recombinant factor. It has been shown to accurately quantities the recombinant factor (http://www.rndsystems.com/Products/DIF57&sta00c/aqQ).
B. Treatment Interventions:
Including (aerobic training 20 minutes, resistive training 15 minutes and flexibility program for 15 minutes), total conventional PT session timing (45 to one hour), 3 times /week for subsequent 3 months.
Cognitive training including the attention/concentration, memory and reaction behavior domains, The time of each cognitive training session(45 to one hour), 3 times /week for consecutive 3 months.
Data Analysis and Statistical Design:
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
40 participants in 2 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal