Skip to content

Comparison the efficacy of eight weeks resistance, balance and combined (resistance- balance) training program on balance, gait and quality of life in patients with Multiple Sclerosis

clinical trial comparing the effect of eight weeks resistance, balance and combined (resistance- balance) training program on balance, gait and quality of life in patients with Multiple Sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017053134257N1
Enrollment
30
Registered
2017-06-15
Start date
2016-07-22
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

multiple sclerosis.

Interventions

in this study we have 3 Exercise interventions. First intervention group performed 8 weeks of Balance exercise for 3 times in week on the supervision of investigator. 2nd intervention group performe
Rehabilitation
in this study we have 3 Exercise interventions. First intervention group performed 8 weeks of Balance exercise for 3 times in week on the supervision of investigator. 2nd intervention group perfor

Sponsors

investivator
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 40 Years

Inclusion criteria

Inclusion criteria: To be eligible for inclusion in the study, participants had to have received a laboratory-supported diagnosis of relapsing-remitting, secondary progressive or primary progressive MS. In addition, they had to meet the following criteria: competence to give informed consent; age between 30 and 40 years; ability to walk 25 feet with or without a cane or bracing; ability to verbalize a willingness to comply with the study's evaluation schedule. The exclusion criteria were as follows: inability to provide informed consent; EDSS score of 7 or higher; inability to walk 25 feet with the use of an assistive device; pregnancy, breastfeeding, or having given birth within 3 months of initiation of the study; diagnosis of any other neurologic disorder or disability that would affect balance and mobility.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Balance, gait and quality of life. Timepoint: balance(Prior to intervention and after 8 weeks intervention); gait (Prior to intervention and after 8 weeks intervention); quality of life(Prior to intervention and after 8 weeks intervention). Method of measurement: Berg balance test, gait distance in 6 minutes and MSQOL-54 questionnaire.

Secondary

MeasureTime frame
None. Timepoint: none. Method of measurement: none.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactamir letafatkar

kharazmi university

letafatkaramir@yahoo.com+98 21 2225 8084

Outcome results

None listed

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