Implementation of a HABIT-ILE Intervention at William Lennox Neurological Hospital (NeuREHA) - Adult

ConditionStroke
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-95
SponsorUniversité Catholique de Louvain

About this trial

Using a randomized controlled trial design, in an hospital environment, possible changes induced by the "Hand-arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE)" treatment program will be investigated in functional activities of daily living, motor and cognitive assessment of patients with sub-acute post-stroke

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Phase aiguë ou subaiguë

Disqualifiers

Epilepsie instable

Absence à déterminer sa volonté à participer

Traitement toxine pendant le stage

Trial design

Design model

Parallel

Treatments tested in this trial

  • HABIT-ILE

    Behavioral

    2 weeks HABIT-ILE

  • Conventional intervention

    Behavioral

    2 weeks usual intervention (waitlist group)

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: HABIT-ILEExperimental treatment 1 intervention
Group B: Conventional InterventionActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Changes on the Adult Assisting Hand Assessment Stroke (Ad-AHA Stroke)

This assessment is an observation-based instrument assessing the effectiveness of the spontaneous use of the affected hand when performing bimanual activities in adults post stroke scored in a logit based 0-100 AHA-unit scale (higher score indicate higher ability)

Time frame
[Time Frame: T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up)]

Secondary outcomes

1

Changes in upper extremities sensorimotor functions assess by the Fugl-Meyer Assessment (FMA-UE)

The FMA-UE assess reflex activity, movement control and muscle strength in the upper extremity of people with post-stroke hemiplegia. Maximum score is 66 points (Higher scores indicates better functioning levels)

Time frame
[Time Frame: T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up)]
2

Changes in unimanual dexterity: Box and Blocks test (BBT)

The BBT is a test of gross manual dexterity. Each hand is tested individually and the BBT is scored through the number of blocks carried over the partition from one part to another part of a box during the one-minute trial period.

Time frame
[Time Frame: T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up)]
3

Changes in Canadian Occupational Performance Measure (COPM)

This is an interview-setting designed to capture a patient's self-perception of performance and satisfaction of it in everyday activities, observed over time. During the interview, parents set up 5 activities considered difficult in daily life. These are then assessed, in a 1 to 10 scale, regarding the child's self-perception of performance and satisfaction of it. The total score is the average of the scores for perception and satisfaction separately (score from 1 to 10; higher score means better performance/satisfaction)

Time frame
[Time Frame: T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up)]
4

Changes in the Stroke Impact Scale (SIS)

Self-reported questionnaire assessing multidimensional repercussions of the Stroke (strength, hand function, daily life activities, mobility, communication, emotion, memory, thinking and participation). Domains are scored on a metric of 0 to 100 (higher scores indicate better self-reported health)

Time frame
[Time Frame: T0 (baseline), T1 (after 2weeks intervention), T2(3 months follow-up)]

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: