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Development and Validity of the Functional Status Assessment Tools in Patients for Rehabilitation

Pilot test and Validation of Functional Assessment tool for activities of daily Living.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002901
Enrollment
500
Registered
2018-05-29
Start date
2013-12-13
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

National Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - brain injury Selection criteria as the subject included those who could be hospitalized for more than 30 days, youth and adults over the age of 13 who could understand the contents of instructions given by the researcher, were capable of speaking, were able to express themselves in writing or drawings, and consented to participate in the research among those diagnosed with brain damages by specialists in rehabilitation medicine and hospitalized. - Spinal cord injury In the case of spinal injury patients, selection criteria as the subject included those who could be hospitalized for more than 30 days, and youth and adults over the age of 13 who consented to participate in the research among those diagnosed with spinal injuries (ASIA damage levels of A, B, C and D) by specialists in rehabilitation medicine and hospitalized.

Exclusion criteria

Exclusion criteria: - brain injury Exclusion criteria in the case of brain damaged patients included those in a medically unstable condition, those with a serious communication disorder that made testing difficult, those with visual or hearing impairment, and those with degraded consciousness. - Spinal cord injury In the case of spinal injury patients, those in a medically unstable condition, and, in the event of accompanying brain damages, patients with unstable systemic conditions due to severe bedsore or urinary tract infection, etc., were excluded.

Design outcomes

Primary

MeasureTime frame
FSAT(ADL independence, Motor function, Sensory function, Cognitive function, Psychosocial funtion)\

Secondary

MeasureTime frame
KSCIM-R;Spastiicity;Coordination;standing balance;linght touch;propriception;k-mmse;Beliefs of Rehabilitation

Countries

Korea, Republic of

Contacts

Public ContactYe Kim

National Rehabilitation Hospital

yesoon@korea.kr+82-2-901-1924

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026