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Effect of Spiritual Training on MS Patients.

Effect of Spiritual Training on Quality of Life on Multiple Sclerosis Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160622028581N2
Enrollment
80
Registered
2018-09-26
Start date
2016-06-21
Completion date
Unknown
Last updated
2018-10-11

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

Conditions

Multiple Sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: The intervention group of Spirituality is grouped in 5 sessions as follows: First session: Introduction of spiritual intervention sessions and familiarization with
Second session: Contact with God
Third session: Contact with yourself
Fourth session: Relationship with Others and Nature and Fifth Session: Explaining the Experience of Spiritual Training and Its Effects and Preparing Members to leave the group and use its achievements

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Introduction to Persian Falconer Age Over 18 Years Confirmed Diagnosis of Multiple Sclerosis Risk Over Three Months From the Time of Diagnosis The Disease is Stage 3-4 Having Poor Quality of LifeScore (Score Between 29 to 58) or Moderate (Score Between ages 58 and 87) Is Not Suffering With Cognitive Disorders or Other Chronic Disease Patients Except for MS Patient Havenot Other Diseases and People Arenot in Acute Phase. Having a Low Score of Spiritual Health (20-40)

Exclusion criteria

Exclusion criteria: Participation in Spirituality Classes Except Current Study Patients Who are Hospitalized During the Study Due to Disease Recurrence If More Than One Session Away

Design outcomes

Primary

MeasureTime frame
Spiritual Health as Another Variable is The Primary Consequence of This Research. Timepoint: Measurement of Spiritual Health of MS Patients in the Beginning of the Study (Before Intervention) and 5 Weeks After (After the Intervention) and 3 Months After the End of the Intervention. Method of measurement: Pulotzin and Ellison Spiritual Health Questionnaire.;Quality of Life Primary outcome Variable. Timepoint: Measurement of Quality of Life of MS Patients in the Beginning of the Study (Before Intervention) and 5 Weeks After (After the Intervention) and 3 Months After the End of the Intervention. Method of measurement: Questionnaire Assessing the `Quality of Life of MS Patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazie Noroozi

Ahvaz University of Medical Sciences

noroozi.r@ajums.ac.ir+98 61 3333 5896

Outcome results

None listed

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