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Treatment of fatigue,depression and paresthesia in Multiple Sclerosis patients

The comparative survey of influence of yoga and aquatic training on fatigue,depression and paresthesia in Multiple Sclerosis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201405188323N8
Enrollment
54
Registered
2014-07-21
Start date
2014-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

fatigue,depression and paresthesia in Multiple Sclerosis patients. Multiple Sclerosis

Interventions

Intervention 1: Yoga group three times a week for two months. Intervention 2: Aquatic training three times a week for two month. Intervention 3: Control group.
Rehabilitation
Yoga group three times a week for two months
Aquatic training three times a week for two month
Control group

Sponsors

Kermanshah University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (Age range 20-50; having EDSS criteria less or equal 6;suffering from fatigue, depression and paresthesia base on FSS criteria, Beck criteria ans SNR criteria;not using effective drugs in fatique, depression and paresthesia; contentment in participating in each of the 3 treatment groups). Exclusion criteria: (severe fatigue, depression and paresthesia that need to be treated by medicine ;patients having Multiple Sclerosis attack in the recent month;patients doing any kinds of sport; patients suffering from concurrent diabetes and cardiac disease, arthritis or psychological diseases).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fatigue,depression,paresthesia in Multiple Sclerosis patients. Timepoint: At the beginning of the first week and at the end of the eighth week. Method of measurement: FSS,Beck,SNR.

Secondary

MeasureTime frame
Change in gate. Timepoint: At the beginning of the first week and at the end of the eighth week. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRazazian Nazanin MD

Kermanshah university of Medical Science

nrazazian@gmail.com+98 83 1427 6310

Outcome results

None listed

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