Kinesiophobia and Balance in Stroke Patients

ConditionStroke
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital

About this trial

This is a cross-sectional clinical study planned to include 138 stroke patients receiving inpatient treatment at the Istanbul Physical Therapy and Rehabilitation Training and Research Hospital.Data on kinesiophobia (Tampa Kinesiophobia Scale-17) , balance performance (Berg Balance Scale) , balance confidence (Activities-specific Balance Confidence Scale-6) , fear of falling (Falls Efficacy Scale) , pain (VAS) , and mood (HADS) will be collected. Clinical and demographic data, including Brunnstrom stages and Barthel Index, will also be recorded. The relationships between these variables will be analyzed statistically.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Voluntary participation in the study

Male and female patients aged 18-80

History of ischemic or hemorrhagic stroke

Functional Ambulation Scale level 3 or higher

Disqualifiers

History of musculoskeletal surgery within the last year

Trauma, fracture, dislocation, or tumor within the last year

Vestibular system disorder

Additional neurological disease that may affect balance (Parkinson's Disease, Multiple Sclerosis, vestibular system disorder)

Trial population

The source population for this cross-sectional study is the adult patient population with a diagnosis of Stroke who are receiving inpatient physical medicine and rehabilitation services in a public training and research hospital setting in Turkey. Specifically, participants will be recruited from the İstanbul Physical Therapy and Rehabilitation Training and Research Hospital inpatient clinic. This setting provides access to a consecutive sample of individuals with varying degrees of functional deficits who are undergoing an organized rehabilitation program.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Survey using a questionnaire.

    Other intervention

    All participants in this single cohort will undergo a one-time, cross-sectional assessment. This assessment includes the collection of clinical and demographic data and the administration of scales for kinesiophobia (Tampa Kinesiophobia Scale-17), balance performance (Berg Balance Scale), balance confidence (ABC-6), fear of falling (Falls Efficacy Scale), pain (VAS), and mood (HADS). No intervention is administered.

Treatment groups

138 Participants
are divided into 1 treatment group
Group A: Inpatient Stroke Survivors1 intervention

Trial outcomes

Primary outcomes

1

Assessment of Kinesiophobia using the Tampa Kinesiophobia Scale-17

The Tampa Kinesiophobia Scale-17 (TKS-17) is a 17-item scale assessing fear of movement. It uses a 4-point Likert scale (1=Strongly disagree to 4=Strongly agree). Items 4, 8, 12, and 16 are reverse-scored. The total score ranges from 17 (minimum) to 68 (maximum). A higher score indicates a higher degree of kinesiophobia.

Time frame
at baseline assessment

Secondary outcomes

1

Berg Balance Scale Score

A 14-item scale assessing postural control. Each item is scored 0 (unable) to 4 (normal performance), with a maximum score of 56.

Time frame
at baseline assessment
2

Falls Efficacy Scale Score

A 10-item scale rating confidence in performing activities on a scale from 1 to 10. Total score ranges from 10 (minimum) to 100 (maximum). Higher scores indicate a higher level of fear of falling.

Time frame
at baseline assessment
3

Hospital Anxiety and Depression Scale Score

A 14-item scale with 7 items for anxiety and 7 for depression, each scored 0-3. Each subscale (Anxiety, Depression) has a maximum score of 21

Time frame
at baseline assessment
4

Barthel Index Score

Assessment of functional independence in activities of daily living.

Time frame
at baseline assessment

Other outcomes

Sponsors and contacts

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