There is no difference in het use of Functional electrical stimulation compared to the use of an ankle foot orthosis in the subacute / post-acute phase after stroke on the recovery of walking ability.
ID
Bron
Verkorte titel
Aandoening
stroke gait functional electrical stimulation
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. 10m Walk Test (10MLT);<br>
2. 6 minutes walk test (6MWT).
Achtergrond van het onderzoek
This study is to identify the effects of a functional elektrical peroneal stimulation (FES) compared to ankle foot orthosis (AFO) on the recovery of walking ability in stroke patients with hemiparesis in the sub/ post-acute phase?
Doel van het onderzoek
There is no difference in het use of Functional electrical stimulation compared to the use of an ankle foot orthosis in the subacute / post-acute phase after stroke on the recovery of walking ability.
Onderzoeksopzet
The participants were evaluated before and immediately after the training program.
Onderzoeksproduct en/of interventie
Participants are randomised to sessions of 30 minutes a day, 5 days a week, for 4 weeks of physiotherapy using either the FES walking aid or the AFO.
Publiek
Erasmus MC / Rijndam Revalidatiecentrum / Libra Zorggroep
M. Kortsmit
Rotterdam
The Netherlands
mkortsmit@hotmail.com
Wetenschappelijk
Erasmus MC / Rijndam Revalidatiecentrum / Libra Zorggroep
M. Kortsmit
Rotterdam
The Netherlands
mkortsmit@hotmail.com
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patients with a first stroke;
2. Subacute phase after stroke (between 4 weeks and 6 months after onset);
3. Age between 18-70 years;
4. Ischemic or hemorrhagic stroke;
5. Hemiparesis;
6. The passive range of motion of the dorsiflexor muscle of the ankle on the hemiparetic side is minimal 5 degrees;
7. Functional ambulation scale score 3.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Cardiac or pulmonary disease that creates a contraindication for physical training;
2. On-demand pacemaker, defibrillator or any electrical or metal implant that could be influenced by the electrostimulation;
3. Malignant tumors;
4. Presence of a fracture or dislocation in the affected leg.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL3716 |
| NTR-old | NTR3879 |
| Ander register | METC Erasmus MC : MEC-2012-021 |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |