Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04718688
Other study ID # M2 COOP_HL
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date June 30, 2018

Study information

Verified date January 2021
Source Hopitaux de Saint-Maurice
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: Acquired brain injury (ABI) in childhood are the cause of disabling motor, cognitive and behavioural disorders, with severe consequences on the later development of autonomy and learning, with long-term repercussions on independence for activities of daily living, and social and professional integration. Among cognitive disorders, executive function (EF) deficits are among the most frequent and disabling, with major consequences on the development of autonomy and the course of schooling and learning. The Cognitive Orientation to daily Occupational Performance (CO-OP) could be an interesting approach for the rehabilitation of these consequences. CO-OP is a performance-based treatment approach for children and adults who experience difficulties performing the skills they want to, need to or are expected to perform. CO-OP is a specifically tailored, active client-centered approach that engages the individual at the meta-cognitive level to solve performance problems. Focused on enabling success, the CO-OP approach employs collaborative goal setting, dynamic performance analysis, cognitive strategy use, guided discovery, and enabling principles. It has been shown to be effective in a variety of populations, but has been little explored in children with ABI. Objectives To assess whether the use of CO-OP could be of interest in children with executive functions deficits following ABI, to improve their occupational performance, their executive functioning in everyday life and their cognitive processes constituting EF.


Description:

Method - Single case experimental study with multiple baselines across individuals and behaviors - 14 individual sessions of CO-OP intervention. - Two goals trained, one control goal. - Different assessments used : Canadian Occupational Performance Measure (COPM), the Goal Attainment Scales (GAS), the Children's Cooking Task (CCT) and parent- and teacher-ratings of the Behavior Rating Inventory of Executive Functions (BRIEF) questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date June 30, 2018
Est. primary completion date June 30, 2018
Accepts healthy volunteers No
Gender All
Age group 8 Years to 14 Years
Eligibility Inclusion criteria were: - Age 8 to 14 years - Diagnosis of ABI, sustained at least 6 months previously, still attending an in- or outpatient rehabilitation program following injury - Evidence of a dysexecutive syndrome on the neuropsychological assessment - Normal vision and hearing (with appropriate correction if necessary) - Sufficient language skills to understand and to communicate explicitly Exclusion criteria were: - Non-French-speaking child or parents - Sensory-motor or visual impairments precluding participation in the study - Intellectual deficit (Full-Scale Intellectual Quotient (IQ)<70), or severe impairments in comprehension, memory or attention, incompatible with understanding and choosing rehabilitation goals and participating in 45-minutes sessions - Neurological, psychiatric, genetic or learning disability diagnosed prior to the ABI - Severe anxiety or depression symptoms

Study Design


Related Conditions & MeSH terms


Intervention

Other:
CO-OP rehabilitation
The intervention was included within the child's conventional rehabilitation program. In the CO-OP original protocol, the child sets 3 goals. Here, we concentrated on two rather than three goals, as addressing three occupations per session seemed too ambitious given the children's cognitive profile (the third goal served as control goal). We chose to increase the number of sessions to 14 (two sessions per week for seven weeks, vs ten in the original protocol). The global strategy was taught to the child at the first session. The following sessions consisted of an iterative process of implementation of the global strategy in the context of guided discovery to identify domain specific strategies to overcome performance ''breakdowns" the children were experiencing when performing the self-selected tasks. In addition, "homework" was assigned to encourage the application and practice. Parents were invited to attend the sessions if it was possible for them.

Locations

Country Name City State
France Saint Maurice Hospitals Saint-Maurice

Sponsors (1)

Lead Sponsor Collaborator
Hopitaux de Saint-Maurice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of Goal Attainment Scaling (GAS) change Goal Attainment Scaling (GAS) is a method for writing personalized evaluation scales in order to quantify progress toward defined goals.
GAS methodology consists in:
Defining a rehabilitation goal;
Choosing an observable behaviour that reflects the degree of goal attainment;
Defining the patient's initial level with respect to the goal;
Defining five goal attainment levels (ranging from a ''no change'' to a ''much better than expected outcome'');
Evaluating the patient after a defined time interval;
Calculating the overall attainment score for all the rehabilitation goals. A five-point scale is used: ''-2'' is the initial pretreatment (baseline) level, ''-1'' represents progression towards the goal without goal attainment, ''0'' is the expected level after treatment, (and therefore, the ''most likely'' level after treatment), ''+1'' represents a better outcome than expected, and ''+2'' is the best possible outcome that could have been expected for this goal.
Baseline to 3-months post-intervention (Three times per week during baseline and intervention phase for each 3 chosen-goal ; one time at 3-months post-intervention)
Secondary Canadian Occupational Performance Measure (COPM) This semi-structured interview helps children/parents identify problematic occupations in different daily areas. COPM will be used: (1) To determine (only with the child) the 4 problematic occupations identified as the most important (3 will be used as target goals, while the 4 will serve as a control goal); (2) To determine changes in occupational performance in self-selected goals: children and parents will rated their performance and satisfaction associated with these 4 occupations. Performance and satisfaction are rated by children and parents on a scale of 1 to 10 (1= not at all able to perform the activity (performance) / not at all satisfied with the way the activity is performed (satisfaction); 10 = perfectly able to perform the activity (performance) / perfectly satisfied with the way the activity is performed (satisfaction). A difference of 2 points between pre- and post-intervention is clinically significant. Before baseline, at immediate post-intervention, at 3-months post-intervention.
Secondary Behavior Rating Inventory of Executive Function (BRIEF) The parent and teacher report forms of the Behavior Rating Inventory of Executive Function (BRIEF, or BRIEF-A for adults'version) provide an ecological assessment of executive functioning through its repercussions in family and school context. Currently, this questionnaire is the best validated and most widely used in children in various congenital, developmental or acquired conditions. The outcome measure is the Global Executive Composite score (GEC) T-Scores (Mean: 50; SD: 10; clinical range cutoff: T-Scores=65). Three times during baseline, at immediate post-intervention, at 1- and 3-months post-intervention
Secondary Children's cooking task The Children's Cooking Task (CCT) is an ecological standardized task designed to assess EF during actual execution of a complex task: the child is asked to prepare a chocolate cake and a fruit cocktail following two simple, highly structured, illustrated recipes with numbered steps. The CCT was used as a secondary outcome measure in this study in order to determine whether children transferred progress in problem-solving, acquired through strategies discovered with CO-OP, onto the performance of a complex task, unrelated to the trained goals. pre-intervention, immediate post-intervention and 3-months post-intervention
See also
  Status Clinical Trial Phase
Completed NCT03911752 - Approach to Sexuality From Occupational Therapy in People With Acquired Brain Injury in Subacute Stage
Completed NCT05265377 - Safety and Usability of the STELO Exoskeleton in People With Acquired Brain Injury and Spinal Cord Injury N/A
Not yet recruiting NCT05863897 - e-COGRAT: A Blended eHealth Intervention for Fatigue Following Acquired Brain Injury N/A
Completed NCT02215590 - Re-Step: Dynamic Balance Treatment of Gait for Acquired Brain Injury (ABI) Victims N/A
Recruiting NCT05309005 - Virtual Reality and Social Cognition After Acquired Brain Injury
Recruiting NCT05443542 - VIrtual Reality in Cognitive Rehabilitation of Processing Speed for Persons With ABI N/A
Recruiting NCT04586842 - Community-based Occupational Therapy Intervention on Mental Health for People With Acquired Brain Injury N/A
Completed NCT03328221 - Physical Activity on Heart Rate Variability in Patients With Severe Acquired Brain Injury
Active, not recruiting NCT05734183 - Multisensorial IMmersive Experiences (MIME) in Disorders of Consciousness N/A
Active, not recruiting NCT05729165 - Local Vibration in Patients With Severe Acquired Brain Injury N/A
Recruiting NCT05440682 - Connectivity in Cranioplasty N/A
Completed NCT04206475 - Feasibility Randomized Trial for an Intensive Memory-Focused Training Program for School Aged Children With Acquired br.Inj. N/A
Recruiting NCT02495558 - Cough Assessment in Patients With Severe Acquired Brain Injury N/A
Completed NCT03989388 - Occupational Self-Analysis Programme N/A
Terminated NCT01974635 - Proprioception Testing in Persons With Sensorimotor Impairment N/A
Not yet recruiting NCT01451242 - The Reliability of Heart Rate Variability Among Patients With Brain Injury as Measured by POLAR RC810XE Compared to HOLTER N/A
Not yet recruiting NCT06058351 - ABI-aftercare in Motion: Multidisciplinary Aftercare in the Home Environment in Patients With Acquired Brain Injury N/A
Completed NCT05052905 - VR-based Remote Rehabilitation for Pediatric ABI N/A
Recruiting NCT06130735 - Impact of Intensive Computerized Cognitive Training N/A
Recruiting NCT04328857 - Experimentation of Sensorized Pseudoelastic Orthoses Produced by Additive Manufacturing N/A