Comparative Analysis of Cryotherapy Combined With Bowen Therapy Versus Medical Massage for Managing Acute Ankle Sprain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Pain Intensity Reduction
研究概览
简要总结
Foot pain is particularly prevalent among older adults, affecting approximately 20% to 37% of men and women aged 45 years and older living in the community. Ankle pain is somewhat less common. This study evaluates the combined impact of cryotherapy (ice application) with Bowen therapy versus traditional medical massage in alleviating symptoms. A total of 41 patients, aged 32-75 years participated and were divided into two treatment groups: one receiving medical massage and ice, and the other Bowen therapy and ice, with three sessions over 15 days. Pain and functionality were measured using the VAS pain scale and Roland-Morris questionnaire. Findings revealed improvements in both groups, with the Bowen therapy group achieving greater pain reduction and functional improvement, suggesting potential advantages of Bowen therapy combined with cryotherapy for managing symptoms.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participants aged 32 to 75 years.
- •Diagnosed with ankle sprain by a qualified healthcare professional (physiatrist or orthopedist).
- •Able to provide informed consent.
- •Willing to comply with the study protocol and attend all scheduled therapy sessions.
排除标准
- •Presence of serious spinal pathologies (e.g., cancer, osteoporosis, trauma, or fracture).
- •History of significant neurological disorders or conditions affecting mobility.
- •Pregnancy or breastfeeding.
- •Previous surgical interventions on the spine or significant other surgeries within the last six months.
- •Current use of medications that affect pain perception (e.g., opioids).
- •Participation in other therapeutic interventions for low back pain during the study period.
结局指标
主要结局
Pain Intensity Reduction
时间窗: 15 days
Pain intensity will be assessed using the Visual Analog Scale (VAS), which allows participants to rate their pain on a scale from 0 (no pain) to 10 (worst possible pain). This measure will be taken at baseline (Day 1) and at the end of the intervention period (Day 15) to evaluate the effectiveness of the interventions in reducing pain levels.
次要结局
- Functional Improvement(15 days)
研究者
Darko Bilic
Director
Rehabilitation Centre Zivot