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The effect Pilates Training on multiple sclerosis

The effect of eight weeks Outdoor and Home-Based Pilates Training on sirtuin1, Chemokine CC ligand 20, serum vitamin D, physical function and some psychological factors in women with multiple sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220316054315N1
Enrollment
44
Registered
2022-03-29
Start date
2022-05-15
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Patients with MS. Multiple sclerosis

Interventions

Intervention 1: Intervention group1: Pilates Exercise Group Outdoors Intervention.15 people will perform an exercise program for eight weeks (three sessions per hour). Intervention 2: Intervention gr

Sponsors

Hakim Sabzevari University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included no smoking, no regular exercise at least two years of history

Exclusion criteria

Exclusion criteria: Muscle injuries, inability to perform exercise severe recurrence of the disease participation in a training program other than the training protocol of research pregnancy recurrence of MS in the last 12 weeks change in MS medication or steroid treatment in 12 weeks Past and period of practice non-cooperation until the end of the research process severe recurrence of the disease

Design outcomes

Primary

MeasureTime frame
Physical function based on 6 minutes walking time. Timepoint: Periods of this study before the intervention and 2 days after the intervention. Method of measurement: Measurement of physical function (cardiorespiratory endurance) by 6-minute walking test.;Investigation of inflammatory status. Timepoint: Measurement of serum cysteine 1 and chemokine 20. Method of measurement: Before intervention and 2 days after intervention.;Check serum vitamin D status. Timepoint: Before intervention and 2 days after intervention. Method of measurement: Examination of blood serum vitamin D by the kit.

Secondary

MeasureTime frame
Assess stress and anxiety. Timepoint: Before the intervention and 2 days after the intervention. Method of measurement: By means of the DASS-21 Stress-Anxiety Questionnaire.;Evaluation of resilience. Timepoint: Before the intervention and 2 days after the intervention. Method of measurement: By Connor-Davidson Resilience Questionnaire.;Evaluation of sleep quality. Timepoint: Before the intervention and 2 days after the intervention. Method of measurement: By Sleep Quality Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactdr roya askari

the Hakim Sabzevari University

vahdatpoor.114@gmail.com+98 51 4401 2763

Outcome results

None listed

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