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The study of the efficacy of the Transdiagnostic Treatment of the Unified for the Improvement of Comorbid Psychological Disorders in Ms Patients

The study of the efficacy of the Transdiagnostic Treatment of the Unified for the Improvement of Comorbid Psychological Disorders (Depression, Anxiety and Health Anxiety), Fatigue and Quality of Life in Patients with Multiple Sclerosis (Ms)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180421039369N2
Enrollment
45
Registered
2019-05-10
Start date
2019-05-19
Completion date
Unknown
Last updated
2019-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

comorbidity of Psychological disorders in Patient with MS. Other specified mental disorders due to brain damage and dysfunction and to physical disease

Interventions

Intervention 1: Intervention group:In this study, the Barlow unified protocol for transdiagnostic treatment method will be used.The sample size in this study is 45. They are randomly divided into two

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Suffering Ms disease with diagnosis of the neurological department Having a score of less than 5 in the (EDSS) Disability Indicator based on a neurologist's assessment to determine the individual's ability to attend a therapeutic session The age range is between 50 to 18 years old Affliction of emotional coexistence disorders including depression, anxiety and health anxiety based on diagnostic interview by psychologist Motivation and satisfaction for participation during treatment and research implementation Failure to receive psychological treatment in the past year Have at least a cycle of educationNot having other chronic diseases such as severe liver disorder The lack of current diagnosis of any mental disorder is consistent in Diagram 1 and 2 based on a psychologist's diagnostic interview, with the exception of emotional disorders including depression, anxiety and health anxiety No obvious risk of suicide now There is no history of drug abuse or dependence at the current time and within one year before the start of treatment

Exclusion criteria

Exclusion criteria: Unwillingness to attend research meetings Not attending at least 50% of the sessions Creating severe physical problems so that it can not be present at meetings

Design outcomes

Primary

MeasureTime frame
Comorbidity of psychological disorders of patients with MS. Timepoint: A week before the intervention, one week after the intervention, Three months after the intervention. Method of measurement: Beck Depression Inventory (BDI-II), Beck Anxiety Inventory, Short form Health Anxiety Scale (SHIA), Fatigue Exercise Scale (FSS), and Quality of Life Scale (MSQOL-54) questionnaire.

Secondary

MeasureTime frame
Depression. Timepoint: A week before the intervention, one week after the intervention, three months after the intervention. Method of measurement: Beck Depression Inventory (BDI-II).;Anxiety. Timepoint: A week before the intervention, one week after the intervention, three months after the intervention. Method of measurement: Beck Anxiety Inventory.;Health Anxiety. Timepoint: A week before the intervention, one week after the intervention, three months after the intervention. Method of measurement: Short Form Health Anxiety Scale (SHIA).;Fatigue Severity. Timepoint: A week before the intervention, one week after the intervention, three months after the intervention. Method of measurement: Fatigue Severity Scale (FSS).;Quality of Life. Timepoint: A week before the intervention, one week after the intervention, three months after the intervention. Method of measurement: Multiple Sclerosis Quality of Life-54 (MSQOL-54).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsasan amiri

Kermanshah University of Medical Sciences

sasanamiri2910@gmail.com+98 84 3442 3968

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026