Fatigue Clinical Trial
Official title:
The Effects of Hot and Cold Compress on Muscle Cramps, Fatigue And Comfort in Hemodialysis Patients: A Placebo Controlled Randomized Trial
Verified date | December 2020 |
Source | Hacettepe University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aims and objectives. To examine and compare the effects of hot and cold compresses administration on muscle cramps, fatigue, and comfort in hemodialysis (HD) patients. Background. Muscle cramps and fatigue are common complications in HD patients and reduce patient comfort. Among the nursing interventions stated for the management of these complications in the literature, hot and cold therapy are remarkable. To the best of our knowledge, the present study is the first research up to date that examined and compared the effects of hot and cold compress administrations on abovementioned complications in HD. Design. This placebo-controlled randomized trial was conducted in two hemodialysis centers between February and October 2020. Methods. The study sample consisted of 69 patients, stratified and randomly allocated to two intervention groups and placebo group. For patients of each group, the implementation of the study continued for four weeks, 12 HD sessions.
Status | Completed |
Enrollment | 69 |
Est. completion date | November 20, 2020 |
Est. primary completion date | October 30, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - between the ages of 18-65, - receiving HD treatment for at least six months, - three days a week with four-hour sessions - with blood pressure 120/80 mmHg and higher at the beginning of the HD session, - did not develop intradialytic hypotension in the first two hours of HD, - hemoglobin value above 8.0 mg/dL, - having a stable dry weight for the previous month (less than 2 kg change). Exclusion Criteria: - receiving intravenous electrolyte replacement during HD session, - having a condition that prevented hot or cold administration such as diabetic neuropathy, burns, open wounds, and amputation in the lower extremities, - with an oncological diagnosis or autoimmune disease (rheumatoid arthritis, systemic lupus erythematosus, ankylosing spondylitis, fibromyalgia, etc.), - refused to participate in the study |
Country | Name | City | State |
---|---|---|---|
Turkey | Hacettepe University | Ankara | None Selected |
Lead Sponsor | Collaborator |
---|---|
Hacettepe University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Comfort | At the end of each hemodialysis session, the comfort level of all participants was measured and recorded using the Hemodialysis Comfort Scale | 4 weeks | |
Primary | muscle cramps | Throughout the hemodialysis treatment, the patients were monitored in terms of cramp development and cramp development was recorded in the follow-up chart (CEFC). This chart was created by the researcher through literature review. Each involuntary contraction session in the legs of the patients was evaluated as an episode. | 4 weeks | |
Secondary | Fatigue | At the end of each hemodialysis session, the fatigue level of all participants was measured and recorded using the Piper Fatigue Scale. | 4 weeks |
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