Kinesiophobia Clinical Trial
Official title:
Investigation of the Relationship Between Depression, Postural Control, Pain, Affected Side and Kinesiophobia in Stroke Patients
NCT number | NCT05538468 |
Other study ID # | 2019/3-22 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 10, 2019 |
Est. completion date | July 30, 2019 |
Verified date | January 2022 |
Source | Inonu University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
It was aimed to determine the presence of kinesiophobia that will affect the treatment in stroke patients and to investigate the relationship between these factors and kinesiophobia by examining factors such as postural control, depression, pain, and affected side that may cause kinesiophobia.
Status | Completed |
Enrollment | 30 |
Est. completion date | July 30, 2019 |
Est. primary completion date | July 15, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 70 Years |
Eligibility | Inclusion Criteria: - individuals who were diagnosed with hemiplegia or hemiparesis after SVO, - at least 6 months after SVO, - who were Level 2 and above according to the Functional Ambulation Classification, - who wanted to participate in the study voluntarily Exclusion Criteria: - Anyone with a major neurological or rheumatological pathology (polyneuropathy, parkinson's, multiple sclerosis, rheumatoid arthritis, etc.) - Affecting the musculoskeletal system other than stroke - Who does not allow mental evaluation, cannot fill in the scales, - is illiterate, has aphasia, has a history of falling, - have any cardiac problems, - amputation in the lower extremities, - those with active malignancy and related chemo/radiotherapy, - the presence of accompanying lower motor neuron or peripheral nerve lesion, - any musculoskeletal problem and related pain (lumbar disc herniation, meniscus, etc.), - individuals with shoulder subluxation, shoulder-hand syndrome - those who refused to participate in the study |
Country | Name | City | State |
---|---|---|---|
Turkey | Inonu University | Malatya |
Lead Sponsor | Collaborator |
---|---|
Inonu University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Kinesiophobia Assessment | VAS Kinesiophobia Assessment were used. The Visual Analog Scale was used as the second method in the assessment of kinesiophobia. A scale is drawn on a 10-centimeter (cm) horizontal line to show the start as 0 (no fear of movement) and the end as 100 (violent fear of movement). They were asked to stand up just before starting the exercise and to mark the severity of the fear of movement they felt at that moment on the scale. | 6 mounts | |
Primary | Kinesiophobia Assessment | Tampa Kinesiophobia Scale were used. The Tampa Kinesiophobia Scale (TKS) is one of them, and it's commonly used in the literature to assess kinesiophobia. It has 17 questions designed to assess fear of moving. | 6 mounts | |
Primary | Pain Assessment | Pain Assessment Visual Analogue Scale (VAS) was used. On a 10-centimeter (cm) horizontal line, start 0 (no pain) and finish 10 (unbearable pain) are marked and the subjects were asked to place a mark on this horizontal line according to the degree of pain they felt. The point marked on the line was then measured with the help of a ruler and recorded as the VAS value in cm. | 6 mounts | |
Primary | Postural Control Assessment | Postural Assessment Scale for Stroke Patients (PASS) was used. The scale, which consists of 12 items, is grouped at 4 different levels (0-3). It is a 2-part scale that assesses the ability to maintain the posture (5 items) and change it (7 items). | 6 mounts | |
Primary | Depression Severity Assessment | Depression Severity Assessment, The Beck Depression Inventory (BDI) was employed, which consists of 21 questions. The scale has a range of 0 to 84 points. | 6 mounts |
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