Skip to content

Goal Attainment Evaluation of Multidisciplinary Telerehabilitation After Traumatic Brain Injury

Goal Attainment Evaluation of Multidisciplinary Telerehabilitation After Traumatic Brain Injury

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04430504
Enrollment
10
Registered
2020-06-12
Start date
2020-11-16
Completion date
2022-02-28
Last updated
2020-11-17

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

Conditions

Traumatic Brain Injury

Keywords

Telerehabilitation, Case series, Traumatic brain injury

Brief summary

The purpose of the study is to evaluate the outcome of a multidiscplinary telerehabilitation after traumatic brain injury assessed by the patient and the therapists with respect to the overall feasibility of the therapy protocol and the effects on psychological well-being and quality of life..

Detailed description

Patients from 18 to 60 years of age recovering after traumatic brain injury are recruited to participate in a multidisciplinary telerehabilitation containing total of 20 video meetings over a period of 4-5 months. The study design consists of a 3-day visit in rehabilitation ward for the pre-treatment clinical assessments and education on the telerehabilitation protocol. A self-exercise program is supervised and monitored using a health platform application on a tablet computer through weekly video meetings. A digital diary recordings enable the therapists to track on the progress of therapies. The primary goal is to achieve the individual goals set in the Goal Attainment Scaling. The secondary goals are related to the improvement of psychological well-being (BDI) and quality of life (WHOQOL-Bref).

Interventions

BEHAVIORALmultidisciplinary telerehabilitation

weekly video meetings to instruct and monitor self-exercises at home

Sponsors

Vetrea Terveys Oy
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Case series of eligible patients

Eligibility

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

Inclusion criteria

* sequelae of traumatic brain injury * capable of doing self exercises at home and participating in video meetings

Exclusion criteria

* moderate or severe aphasia * poor recovery potential for return to school or working life based on clinical assessment

Design outcomes

Primary

MeasureTime frameDescription
Goal Attainment Scaling20 weeksOutcome scaling: -2 (worse expected outcome), -1 (less than expected outcome), 0 (expected outcome), +1 (more than expected outcome), +2 (best expected outcome)

Secondary

MeasureTime frameDescription
Beck Depression Inventory20 weeks21-question inventory to yield a total score 0-63: 0-13 (no depression), 14-19 (mild depression), 20-28 (moderate depression), 29-63 (severe depression)
WHOQOL-Bref20 weeks26-item instrument consisting of four domains: physical health (7 items), psychological health (6 items), social relationships (3 items), and environmental health (8 items). Each domain scoring 0-100 (0 = worst, 100= best possible) to compare with age-related mean values.

Countries

Finland

Contacts

Primary ContactKauko Pitkänen, MD, PhD
kauko.pitkanen@vetrea.fi0505965289

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026