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Tele-rehabilitation with tailored exercise program to patients with Chronic inflammatory demyelinating polyneuropathy (CIDP) and Guillain-Barre Syndrome: Randomised clinical trial

Tele rehabilitation with tailored exercise program to patients with Chronic inflammatory demyelinating polyneuropathy (CIDP) and Guillain-Barre Syndrome: Randomise clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210622005
Enrollment
60
Registered
2021-06-22
Start date
2021-09-08
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Motor and sensory disorders associated with CIDP and GBS CIDP GBS AIDP AMSAN Physical therapy Physical therapist Modalities, physical therapy Physiotherapy physiotherapy techniques Exercise Physical exertion Physical exercise Physical activity Physical fitness Aerobic training Resistance training Aerobic exercise Resistance exercise Rehabilitation Rehabilitation programme Intervention Rehabilitation intervention Quality of life Fatigue Activities of daily living Muscle strength Telerehabilitat

Interventions

A tailored exercise program will be given to the participants. Twice a week for 12 weeks, the program will be adjusted depending on the patients&#039
needs.,The patients will be evaluated and they will be given general advice for exercise and physical activity. They will have no further contact with the research team.
Experimental Other,Experimental Other
Tailored exercise program with telerehabilitation ,Advice for exercise

Sponsors

National and Kapodistrian University of Athens, Greece
Lead Sponsor
Physiotherapy Department, Laboratory of Neuromuscular and Cardiovascular Study of Motion, University of West Attica, Greece
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. they must be 18 years of age or more 2. they must be diagnosed with CIDP or GBS 3. they do not follow any other activity plans 4. they have a stable medication (that follow for the past 2 months) 5. they can consent 6. they can communicate

Exclusion criteria

Exclusion criteria: 1.They are unable to walk or they cannot walk for more than 10 meters on their own 2.They have serious vision/auditory issues that hinder their ability to communicate 3. They have serious conditions, that do not allow them to participate in exercise programs 4. They are cancer patients 5. They have recently undergone surgery, less than 12 months since surgery date 6. They suffer from alcoholism 7. They suffer from drug abuse

Design outcomes

Primary

MeasureTime frame
Physical Activity 1st before the intervention, 2nd after the end of the intervention and 3rd 3 months after the intervention. NSS,NDS, INCAT Dissabilities Scale,NRS score ,Gate assessment 1st before the intervention, 2nd after the end of the intervention and 3rd 3 months after the intervention. 1.10m Walk Test 2. Berg Balance scale,Fatigue assessment 1st before the intervention, 2nd after the end of the intervention and 3rd 3 months after the intervention. 1.Fatigue Severity Scale (F.S.S ) 2.Symptom Rating Scale for Depression and Anxiety

Secondary

MeasureTime frame
Quality of Life 1st before the intervention, 2nd after the end of the intervention and 3rd 3 months after the intervention. Medical Outcomes Study (MOS) short-form health survey 36 Item (SF-36)

Countries

Greece

Contacts

Public ContactMagdalini Stamou

Univercity of West Attica

mstamou@uniwa.gr00306973301540

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026