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

Phase 1

• Conditions: Motor and sensory disorders associated with CIDP and GBS; CIDP; GBS; AIDP; AMSAN; Physical therapy; Physical therapist; Modalities, physical therapy; Physiotherapy; physiotherapy techniques

• Registration Number: TCTR20210622005
• Lead Sponsor: ational and Kapodistrian University of Athens, Greece

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-06-22
• Study Completion: 2022-05-16
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 60

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

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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)