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Comparison of the outcomes of home based and supervised individually designed exercise programme amongst the patients in chronic phase after Guillain Barre syndrome.

A Study to compare the Outcomes of Home Based and Supervised Individually Designed Exercise Programme for Patients in Chronic Phase after Guillain Barre Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/08/007150
Enrollment
62
Registered
2016-08-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Guillain Barre syndrome

Interventions

Intervention1: Supervised individually designed exercise programme: The supervised physiotherapy programme will include up to three one- hour interrupted physiotherapy session per week for strengtheni

Sponsors

Bhopal Memorial Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients above 18 years of age of â??definiteâ?? GBS diagnosed through World Health Organization of International Classification of Disease, having current stable medical course within last five years and all new cases, confirmed by physician/neurologists. We shall include only those participants who have a physical disability as assessed by the International Classification of Impairment, Disability and Handicap (WHO 1980) was updated by the World Health Organization to the International Classification of Functioning, Disability and Health (WHO 2001), as an international standard to describe health and disability Clinical judgement of the assessing physician/ physiotherapist regarding potential benefits of the physiotherapy programme to the individual. All variants of GBS will be included in the study.

Exclusion criteria

Exclusion criteria: Patient those who have received the physiotherapy treatment in the period of previous 6 months.

Design outcomes

Primary

MeasureTime frame
Functional impairment measurementTimepoint: At the time of recruitment, at six months, at 12 months

Secondary

MeasureTime frame
Fatigue Severity Scale,MRC manual muscle testing, Visual analog scale for pain, Barthel Index for activities of daily living, World Health Organization Quality of LifeTimepoint: at the time of recruitment, at six months, at 12 months

Countries

India

Contacts

Public ContactNehal Shah

Bhopal Memorial Hospital and Research Center

nehalravirajshah@rediffmail.com9424442993

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 24, 2026