Quality of Life Clinical Trial
Official title:
The Effect of Kinesiophobia on Spatio-temporal and Functionality in Individuals Who Have Undergone Total Knee Replacement Surgery
Verified date | March 2020 |
Source | Firat University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
It is stated that after arthroplasty surgery, besides the physiological factors, the factors
related to the individuals may affect the recovery. Among these factors, one of the most
defined in the literature is kinesiophobia. Although kinesiophobia is defined as the terms of
"fear of movement" and "fear related to pain"; There are also definitions for situations in
which fear of movement is most extreme or pain-related fear avoidance beliefs. Kinesiophobia,
which usually occurs in the preoperative period and supports the development of chronic pain,
may also affect the early recovery findings. It is very important to determine the presence
and severity of kinesiophobia as it is associated with functional results after surgery.
Individuals' perceptions about themselves, expectations of recovery, and personal beliefs
before surgery are thought to affect recovery in the early period. In the studies conducted,
it was stated that individuals with high perception about himself and the surgical process
recover faster and return to activities. However, it is emphasized that studies should be
conducted on the effect of individuals' personal factors such as self-efficacy,
self-perception and their perspective on health on the healing process.
Status | Enrolling by invitation |
Enrollment | 2 |
Est. completion date | May 15, 2020 |
Est. primary completion date | March 15, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
- Inclusion Criteria: - Between 30-90 years old, - Primary unilateral total knee replacement will be applied due to knee osteoarthritis, - Patients volunteering to participate in the study - Exclusion Criteria: - Who have neurological (hemiplegia, parkinson, multiplsclerosis etc.) disease that will affect functional performance and balance, - Does not have cognitive function to allow active participation, - Having a severe psychiatric condition, - Severe vision and hearing loss, - Any other treatment other than medication, - Who have contralateral knee osteoarthritis (pain with activity 4/10 or higher), - Using drugs that can cause loss of balance, - With more than 5 cm length difference in the lower extremities, - Having undergone lower limb trauma or surgery in the past 1 year, |
Country | Name | City | State |
---|---|---|---|
Turkey | Firat Univerity Hospital | Elazig |
Lead Sponsor | Collaborator |
---|---|
Firat University |
Turkey,
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Güney-Deniz H, Irem Kinikli G, Çaglar Ö, Atilla B, Yüksel I. Does kinesiophobia affect the early functional outcomes following total knee arthroplasty? Physiother Theory Pract. 2017 Jun;33(6):448-453. doi: 10.1080/09593985.2017.1318988. Epub 2017 May 8. — View Citation
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Tampa Scale of Kinesiophobia | Evaluation will be done before surgery .Individuals' kinesiophobia will be evaluated | 2 weeks | |
Primary | The Tampa Scale of Kinesiophobia | Evaluation will be done before surgery at the 1st month.Individuals' kinesiophobia will be evaluated | 1 mounth | |
Primary | The Tampa Scale of Kinesiophobia | Evaluation will be done before surgery at the 3st month. Individuals' kinesiophobia will be evaluated | 3 Mounth | |
Secondary | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) | Evaluation will be done before surgery, Pain, joint stiffness and function data will be evaluated. | 2 weeks | |
Secondary | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) | Evaluation will be done before surgery, at the 1st months. Pain, joint stiffness and function data will be evaluated. | 1 mounth | |
Secondary | The Western Ontario and McMaster Universities Arthritis Index (WOMAC) | Evaluation will be done before surgery, at the 3rd months. Pain, joint stiffness and function data will be evaluated. | 3 mounth | |
Secondary | Spatio-temporal gait | Evaluation will be done before surgery. The data will be made with the Win-Track walking platform. | 2 weeks | |
Secondary | Spatio-temporal gait | Evaluation will be done before surgery, at the 1st. The data will be made with the Win-Track walking platform. | 1 mounth | |
Secondary | Spatio-temporal gait | Evaluation will be done before surgery, at the 3rd months. The data will be made with the Win-Track walking platform. | 3 mounth | |
Secondary | Lequesne Index | Evaluation will be done before surgery. It is a 10-item scale consisting of 3 sections: pain / discomfort, daily life activities and maximum walking distance. | 2 weeks | |
Secondary | Lequesne Index | Evaluation will be done before surgery, at the 1st. It is a 10-item scale consisting of 3 sections: pain / discomfort, daily life activities and maximum walking distance. | 1 mounth | |
Secondary | Lequesne Index | Evaluation will be done before surgery, at the 3rd months. It is a 10-item scale consisting of 3 sections: pain / discomfort, daily life activities and maximum walking distance. | 3 mounth | |
Secondary | Hormone level of iris | Evaluation will be done before surgery.Blood samples will be taken into gel biochemistry tubes, as appropriate for analysis from patients. The blood collected will be centrifuged for 10 minutes at 3000 rpm and the serum will be separated and the obtained serums will be placed in ependorphic tubes in small portions and stored at -80 ° C until analysis. The levels of iris will be studied in accordance with the kit user manual using commercial ELISA (enzyme-linked immunosorbent assay) kits. | 2 weeks | |
Secondary | Hormone level of iris | Evaluation will be done before surgery, at the 1st. Blood samples will be taken into gel biochemistry tubes, as appropriate for analysis from patients. The blood collected will be centrifuged for 10 minutes at 3000 rpm and the serum will be separated and the obtained serums will be placed in ependorphic tubes in small portions and stored at -80 ° C until analysis. The levels of iris will be studied in accordance with the kit user manual using commercial ELISA (enzyme-linked immunosorbent assay) kits. | 1 Mounth | |
Secondary | Hormone level of iris | Evaluation will be done before surgery, at the 3rd months. Blood samples will be taken into gel biochemistry tubes, as appropriate for analysis from patients. The blood collected will be centrifuged for 10 minutes at 3000 rpm and the serum will be separated and the obtained serums will be placed in ependorphic tubes in small portions and stored at -80 ° C until analysis. The levels of iris will be studied in accordance with the kit user manual using commercial ELISA (enzyme-linked immunosorbent assay) kits. | 3 Mounth |
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