The Effect of Propolis in Tinea Pedis Treatment: A Randomized Controlled Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 96
- 试验地点
- 2
- 主要终点
- Evaluation
研究概览
简要总结
Tineapedis is an important health problem. Providing foot care in tinea pedis treatment contributes positively to the treatment. In addition, alternative treatments can also be used. In this study, the randomization study group will be divided into three. Medical treatment and foot care training will be applied to the first group, medical treatment and propolis to the second group, medical treatment and plassebo to the control group. Foot care training will be given by nurse coaching. Times of all three groups and their response to treatment will be evaluated.
详细描述
- Study Identification: Randomised Controlled Trial
- Study Status: This will begin
- Sponsor/Collaborators: SBS Scientific Bio Solutions Inc.
- Oversight: Patients will be given foot care training. At the same time, a phone call will be provided by the research nurse every week. Evaluation will be made at the end of 2 months
- Study Description
It was planned as a double-blind randomized controlled study. The person conducting the randomizer, the person making the statistics and the person performing the medical examiner will be blinded. Power analysis was made using the G * Power (3.1.9.4) program, 0.05 margin of error and 85% power were accepted. A total of 96 people were divided into three groups. Groups were composed of 36 people, including 10% losses for each group.
Inclusion Criteria:
Not being pregnant Not being breastfeeding Not having confusion Not being immunosuppressed Not using systemic cortisone Not having any dermatological problems (psoriasis, contact dermatitis, etc.) that will affect the treatment.
Agree to participate in research Being accessible by phone Having no problems communicating by phone Not having problems with physical care
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Not being pregnant
- •Not being breastfeeding
- •Not having confusion
- •Not being immunosuppressed
- •Not using systemic cortisone
- •Not having any dermatological problems (psoriasis, contact dermatitis, etc.) that will affect the treatment.
- •Agree to participate in research
- •Being accessible by phone
- •Having no problems communicating by phone
- •Not having problems with physical care
排除标准
- •Pregnant / nursing women
- •Using systemic antifungal therapy
- •Using systemic croticosteroids
- •In the process of treatment for oncological reasons
- •Are using immunosuppressants
- •Dermatological disease (contact dermatitis, psoriasis)
- •Under the age of 18 and over the age of 64
- •Have cognitive problems
- •There is no telephone / telephone number within reach
- •Individuals who have difficulties in speaking and understanding Turkish will be excluded from the study.
结局指标
主要结局
Evaluation
时间窗: 3 month
Dermatological Quality of Life Scale
次要结局
- Doctor's an patient's global(3 month)
研究者
Rukiye Burucu
Assit. Prof.
Necmettin Erbakan University