Clinical Monitoring Using ICF

NCT06753877 | Completed

• 1 other identifier: HÜ-OT-LKO-02
• Study Type: interventional
• Target: 200
• Locations: 1 country
• Sites: 1

Brief Summary

The present study examined stroke patients who applied to occupational therapy units within the framework of ICF, following the rehabilitation process, and defining frequently used measurements in terms of ICF codes

Conditions

Stroke

Keywords

stroke; activities of daily living; participation; rehabilitation

Outcome Measures

Primary Outcomes (1)

• Functional Independence Scale (FIM)

  The FIM is a scale that measures a person's level of independence in basic motor and cognitive activities of daily living. It consists of 18 items and assesses 2 sub-areas. 1) motor function and 2) cognitive function. Each item is scored on a detailed scale ranging from 1 to 7 (level 1 = fully dependent, level 7 = fully independent). The total score ranges from 18 to 126. The higher the person's score, the higher the level of independence (Ravaud et al., 1999). The Turkish cultural adaptation study was conducted.

  1 month

Secondary Outcomes (1)

• Mini Mental State Examination (MMSE)

  1 month

Other Outcomes (3)

• Stroke Impact Scale version 3.0 (SIS v-3.0):

  1 month

• Lawton-Brody Instrumental Activities of Daily Living (Lawton-Brody IADL)

  1 month

• Frenchay Activities Index (FAI):

  1 month

Study Arms (1)

Aspirin (single group)

EXPERIMENTAL

The present study has one group. Holistic rehabilitation service was provided to all individuals. The program involved different therapies. Participants were given standard physiotherapy services (electrotherapy, exercise, gait training, hydrotherapy, respiratory therapy) and standard occupational therapy services. Occupational therapy interventions were provided by the researchers.

Behavioral: holistic rehabilitation

Interventions

holistic rehabilitation BEHAVIORAL

Holistic rehabilitation service All participants in the study were cared for in the inpatient unit. The same physician and nurses followed the participants for 1 month. The participants were regularly taking their medication and had no co-morbidities. All participants stayed in double rooms and all stayed with their caregivers. The assessments were carried out within the first 3 days of admission to the inpatient unit. The second assessments were repeated by the same professional. Rehabilitation interventions were provided by different therapists. Participants were given standard physiotherapy services (electrotherapy, exercise, gait training, hydrotherapy, respiratory therapy) and standard occupational therapy services. Occupational therapy interventions were provided by the researchers. Physiotherapy services were provided by physiotherapists working full-time in the hospital. Physiotherapy was provided 5 days a week and occupational therapy was provided 3 days a week.

Aspirin (single group)

Eligibility Criteria

• Age: 18 Years - 64 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Diagnosis of stroke, age between 18 and 64 years,
• Being served by hospital, being enrolled in the occupational therapy,
• Volunteering to participate in the study

You may not qualify if:

• Individuals with orthopedic, psychological or neurological conditions other than stroke that could affect their functioning and those with moderate or severe aphasia were not included in the study

Sponsors & Collaborators

• Hacettepe University: lead

Study Sites (1)

Mardin Traning and Rsearch Hospital

Mardin, Artuklu, 47060, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular Disorders; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Vascular Diseases; Cardiovascular Diseases

Study Officials

• leyla kaya öztürk, MSc

  Mardin Training and Research Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Masking Details: The therapist who conducted the assessment tests was unaware of the study design.
• Purpose: BASIC SCIENCE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Model Details: One group was investigated within the ICF framework

Study Record Dates

• First Submitted: December 23, 2024
• First Posted: December 31, 2024
• Study Start: June 1, 2024
• Primary Completion: October 1, 2024
• Study Completion: December 19, 2024
• Last Updated: December 29, 2025

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)