Efficacy of Craniosacral Therapy in the management of Plantar Fasciitis: A Randomized Controlled Trial
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 52
- 试验地点
- 1
- 主要终点
- Visual Analog Scale (VAS) for the pain assessment.
研究概览
简要总结
Plantar fasciitis is one of the most common causes of heel pain, often resulting in functional limitations and reduced quality of life. Conventional physiotherapy, including stretching, strengthening, ultrasound therapy, and patient education, has been widely used in its management. Craniosacral therapy (CST) is a gentle manual therapy technique that aims to release fascial restrictions and restore balance in the craniosacral system, which may influence musculoskeletal structures through fascial and neural connections. However, its role in plantar fasciitis management remains underexplored.
The present randomized controlled trial is designed to evaluate the efficacy of craniosacral therapy in addition to conventional physiotherapy compared to conventional physiotherapy alone. Individuals clinically diagnosed with plantar fasciitis will be screened based on inclusion and exclusion criteria. Eligible participants will provide informed consent and will then be randomly allocated into two groups using a computer-generated randomization method.
Group A will receive CST along with conventional physiotherapy, while Group B will receive only conventional physiotherapy. Each intervention session will last 40–45 minutes and will be conducted three times per week for two consecutive weeks, totaling six sessions.
Outcome measures will be assessed at baseline and after two weeks. These will include pain intensity (Visual Analogue Scale), foot function (Foot Function Index), ankle range of motion (goniometer), and muscle strength of tibialis anterior and gastrocnemius–soleus (Manual Muscle Testing). All assessments will be carried out by a blinded assessor.
This trial will help determine whether craniosacral therapy provides additional benefit over conventional physiotherapy in reducing pain and improving functional outcomes in individuals with plantar fasciitis.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)(—)
- 性别
- All
入选标准
- •Adults above 18 years of age diagnosed with plantar fasciitis.
- •Duration of heel pain more than 3 months.
- •Positive Windlass test or pain reproduced on passive toe extension.
- •Tenderness along the plantar fascia on palpation.
- •Reduced ankle mobility.
- •Not undergoing any current physiotherapy or other treatment for plantar fasciitis.
排除标准
- •Current undergoing physiotherapy treatment for plantar fasciitis.
- •Use of medications such as NSAIDs or analgesics for heel pain within the last 2 weeks.
- •Patients already performing self-massage, stretching, or home-based exercises for plantar fascia.
- •Past history of stroke, recent head injury, skull fractures, aneurysm, or other contraindications to Craniosacral Therapy (CST).
- •Patients currently undergoing Craniosacral Therapy or similar manual therapy interventions.
结局指标
主要结局
Visual Analog Scale (VAS) for the pain assessment.
时间窗: Pretest (Before starting the tretment protocol at 0 day) and Post test (After the complition of tretment protocol at 12th day)
Universal Goniometer for the Range of motion assessment of ankle joint.
时间窗: Pretest (Before starting the tretment protocol at 0 day) and Post test (After the complition of tretment protocol at 12th day)
次要结局
- Foot Function Index to check the functional disability.(Pretest (Before starting the tretment protocol at 0 day) and Post test (After the complition of tretment protocol at 12th day))
- Manual Muscle Testing to check the muscle strength(Pretest (Before starting the tretment protocol at 0 day) and Post test (After the complition of tretment protocol at 12th day))
研究者
Dr Varun Kalia
Lovely Professional University
