Hemodialysis Patients Clinical Trial
Official title:
The Effect of Local Aromatherapy Applied to Hemodialysis Patients Before Arterio-venous Fistula Cannulation on Pain, Anxiety and Satisfaction
Verified date | April 2024 |
Source | TC Erciyes University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The most active members of the healthcare professionals responsible for hemodialysis units are nurses, and they have a key role in pain, anxiety and satisfaction management as they are responsible for cannulation. Therefore, complementary and integrated practices need to be implemented based on evidence to strengthen the independent role of nurses in managing pain and anxiety.
Status | Active, not recruiting |
Enrollment | 60 |
Est. completion date | June 30, 2024 |
Est. primary completion date | June 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Those who are over 18 years of age, - Able to answer questions and communicate, - No hearing, vision or speech impairments, - Regularly undergoing hemodialysis three times a week, - Having arterio-venous fistula for at least 3 months, - Having pain during needle cannulation and scoring at least two or more points on the Visual Analogue Scale (VAS), - Having been on hemodialysis for at least three months, - Agreeing to participate in the study with their own consent, - Patients who are not allergic to clove oil will be included in the study. Exclusion Criteria: - Having neuropathic pain, - Patients with arterio-venous fistula and loss of sensation of more than 50% in the extremity, - Patients with infection in the arterio-venous fistula line, - Patients with aneurysm or pseudoaneurysm in arterio-venous fistula, - Patients who have used analgesic medication/s in the last 6 hours, - Patients who have used sedative agent(s) in the last 6 hours, - Patients who used local anesthetic agents before needle intervention will not be included in the study. |
Country | Name | City | State |
---|---|---|---|
Turkey | Erciyes University | Melikgazi | Kayseri |
Lead Sponsor | Collaborator |
---|---|
TC Erciyes University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analog Scale (VAS) | This scale will be used in our study to evaluate the anxiety experienced by patients before needle cannulation and the pain and satisfaction experienced after needle cannulation. | before and after the intervention, for 1 month, 12 times | |
Secondary | State and Trait Anxiety Inventory (STAI) | In our study, this scale will be used to evaluate the anxiety that patients may experience due to cannulation. | before and after the study, for 1 month, 2 times |
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