Mind-body interventions in patients with multiple sclerosis

Not Applicable

Completed

• Conditions: Multiple sclerosis; Neurological - Multiple sclerosis

• Registration Number: ACTRN12618002024224
• Lead Sponsor: Aniel Jessica Leticia Brambila Tapia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2018-08-24
• Study Start: 2018-12-18
• Last Update Posted: 14 June 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 7

Inclusion Criteria

Patients older than 18 years
Patients with multiple sclerosis diagnosed with the McDonald criteria
Patients with walking limitation, with at least 6 points in the Expanded disability status scale (EDSS score equal or more than 6)
Patients that want voluntarily participate in the study

Exclusion Criteria

Patients with cognitive impairment that prevent to perform the interventions

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient functionality measured by the expanded disability status scale. [this variable was measured 1 week before the first intervention and 1-2 weeks after the last intervention and in a follow up 3 months later.];the primary caregivers were measured for anxiety state and trait with the State-Trait Anxiety Inventory (STAI) [this variable was measured 1 week before the first intervention and 1-2 weeks after the last intervention and 3 months later.];For primary caregivers: The Zarit burden inventory[This variable was measured 1 week before the first intervention and 1-2 weeks after the last intervention and 3 months later]

Secondary Outcome Measures

Name	Time	Method
The quality of life measured with the short form 36 health questionnaire, SF-36[this variable was measured 1 week before the first intervention and 1-2 weeks after the last intervention and in a follow up 3 months later.]