Ataxia Clinical Trial
— ASPECTOfficial title:
The ASsessment and Physiotherapy managEment of Ataxia in Children Following Surgical Resection of Posterior Fossa Tumour (ASPECT)
NCT number | NCT03945682 |
Other study ID # | 227917 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | March 5, 2018 |
Est. completion date | December 31, 2020 |
The overall aim of the study is to determine the feasibility of conducting a randomised controlled trial (RCT) studying the effectiveness of physiotherapy intervention (virtual training) in children with ataxia following surgical resection of posterior fossa tumour
Status | Recruiting |
Enrollment | 40 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 4 Years to 18 Years |
Eligibility |
Inclusion Criteria: - Child or young person (4-<18 years) demonstrating ataxia. (For this study, ataxia is currently defined as SARA greater than 2. This definition is taken from data from the CARS study to date, from the cut off threshold value distinguishing no ataxia from mild ataxia) - 12 months to 3 years following surgical resection of posterior fossa tumour. (This time frame has been selected as this covers the time when the children will typically have completed any adjunct oncology treatment and therefore more emphasis is dedicated to rehabilitation). Exclusion Criteria: - Medically unstable/currently undergoing adjunctive treatment e.g. radiotherapy or chemotherapy - Less than 4 years of age (due to inability to complete standardized assessments) - Aged 18 or over - Unable to stand independently for less than one minute or SARA gait item score over 4, either of which would inhibit capacity to complete the training session. - Presence of co-morbities with the potential to affect the safety of training, such as congenital or acquired disorders causing high risk of falls or lack of comprehension of training tasks, or current musculoskeletal impairments (such as a non-union fracture or fracture currently healing limiting weight-bearing) |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Alder Hey Children's NHS Foundation Trust | Liverpool | Merseyside |
Lead Sponsor | Collaborator |
---|---|
Alder Hey Children's NHS Foundation Trust |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Process Measures | Number of patients identified who meet the inclusion criteria and are then subsequently recruited will be recorded. | 32 months | |
Primary | Intervention Process Measures | Number of patients who complete all sessions of the intervention will be recorded and the patient's adherence to treatment in the home setting will be noted. | 32 months | |
Secondary | SARA | Scale for the Assessment and Rating of Ataxia | 32 months | |
Secondary | BARS | Brief Ataxia Rating Scale | 32 months | |
Secondary | 9HPT | Nine hole peg test | 32 months | |
Secondary | PEDI | Paediatric Evaluation of Disability Index | 32 months | |
Secondary | PedsQL | Brain Tumour Module | 32 months | |
Secondary | BBS | Berg Balance Scale | 32 months | |
Secondary | INAS | Inventory of Non Ataxia Signs. Assessment of compliance (diary) | 32 months | |
Secondary | Subjective Impact | Subjective Impact Likert Scale | 32 months |
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