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Participation and Executive Functions in Adults Following Traumatic Brain Injury In Sub-Acute Inpatient Rehabilitation

Participation and Executive Functions in Adults Following Traumatic Brain Injury During Suba-Acute Inpatient Rehabilitation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04292925
Enrollment
40
Registered
2020-03-03
Start date
2020-03-01
Completion date
2023-12-31
Last updated
2023-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury

Keywords

Executive functions, cognitive, sub-acute, rehabilitation

Brief summary

Aim: To examine the feasibility of a new treatment protocol in improving executive function deficits and participation in daily activities of adults with TBI at discharge and one month post-discharge. A double-blind (assessors) randomized control trial (RCT) with two groups, experimental and control. This study will include 40 adults hospitalized in the inpatient Head Trauma unit. Potential patients will be approached by occupational therapists working in the inpatient Head Trauma rehabilitation unit and be invited to participate in the study. If they agree, they will be asked to sign an informed consent form. Then they will undergo a screening assessment. Participants who are found eligible will be then administered a cognitive assessment battery. Then they will be randomly allocated to either the experimental (new treatment protocol) or the control (conventional therapy) group. In both groups, the intervention will include 18 treatment sessions of 45 minutes, between three to five times a week depending on the participant's state, over a period of four to six weeks. Following the intervention, participants will undergo the assessment again. Participation questionnaires will be administered by telephone one month post-discharge.

Detailed description

A double-blind randomized control trial (RCT) with two groups, experimental and control. This study will include 40 adults hospitalized in the inpatient Head Trauma unit. Potential patients will be approached by occupational therapists working in the inpatient Head Trauma rehabilitation unit and be invited to participate in the study. If they agree, they will be asked to sign an informed consent form. Then they will undergo a screening assessment. Participants who are found eligible will be then administered a cognitive assessment battery. Then they will be randomly allocated to either the experimental (new treatment protocol) or the control (conventional therapy) group. In both groups, the intervention will include 18 treatment sessions of 45 minutes, between three to five times a week depending on the participant's state, over a period of four to six weeks. Following the intervention, participants will undergo the assessment again. Participation questionnaires will be administered by telephone one-month post-discharge.

Interventions

OTHERNew treatment protocol

The new treatment protocol focuses on training of executive processes using remedial strategies and on promoting the use of meta-cognitive strategies. Goal directed activities are used to improve the underlying cognitive process and transfer of the learned skill to everyday function will be encouraged.

OTHERConventional therapy

conventional therapy

Sponsors

Loewenstein Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Mild to severe TBI as diagnosed by a physician and confirmed by imaging * age 18-60 * able to understand instructions of assessment tools as will be determined by their Occupational Therapist * basic cognitive abilities preserved as will be determined by three subtests of the Loewenstein Occupational Therapy Cognitive Assessment: orientation (score: 6/8 or above), visual perception (score: 3/4 or above) and spatial perception (score: 2/4 or above) * at least one functional upper extremity as will be determined by their Occupational Therapist * intact or corrected vision. * a score of 1 or above in the The Multiple Errands Test - the hospital version (MET-HV).

Exclusion criteria

* epilepsy * history of drug use * other psychiatric or neurologic disorder.

Design outcomes

Primary

MeasureTime frameDescription
The Multiple Errands Test - the hospital version (MET-HV)30 minutesA performance-based assessment which was design to assess the effect of EF deficits on everyday functioning.

Secondary

MeasureTime frameDescription
Cognitive Self Efficacy Questionnaire II (CSEQ)15 minutesThe CSEQ is a questionnaire designed to assess a person's beliefs regarding their ability to recognize, monitor and manage cognitive symptoms and everyday challenging cognitive activities.
Self-Perceptions in Rehabilitation Questionnaire (SPIRQ)15 minutesThe SPIRQ is a 20 items questionnaire designed to measure clients' self-perceptions of injury, perceived benefits of rehabilitation, and emotional reactions throughout inpatient or outpatient rehabilitation.
Mayo-Portland Adaptability Inventory - 4 (MPAI-4)15 minutesThe MPAI is designed to assist in the clinical evaluation of people during post acute period following traumatic brain injury, to assist in the evaluation of rehabilitation programs and to better understand the long-term outcomes of traumatic brain injury.
Quality of Life After Brain Injury (QOLIBRI)15 minuteIs a questionnaire designed to assess quality of life following traumatic brain injury. The QOLIBRI instrument consists of 37 items in four satisfaction scales, ''Cognition'' (7 items), ''Self'' (7 items), ''Daily Life and Autonomy'' (7 items), and ''Social Relationships'' (6 items), and two bothered scales, ''Emotions'' (5 items) and ''Physical Problems'' (5 items).
WebNeuro neurocognitive assessment battery30 minutesA web-based computerized battery of neurocognitive functioning.

Other

MeasureTime frameDescription
Loewenstein Occupational Therapy Cognitive Assessment (LOTCA)30 minutesThe LOTCA was designed to give a preliminary cognitive profile for patients with an acquired head injury
Functional Independence Measure (FIM)15 minutesThe FIM instrument is designed to assess functional independence. The FIM consists of 18 items which are divided into six subscales (self-care, sphincter control, transfers, locomotion, communication, and social cognition). Each of the 18 items have a maximum score of 7 (complete independence) and a minimum score of 1 (complete dependence), thus possible scores range from 18 to 126 (Donaghy & Wass, 1998).

Countries

Israel

Contacts

Primary ContactRotem Eliav
rotemeliav1@gmail.com+972543020023

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026