Effect of Phonophoresis Versus Iontophoresis in the Treatment of Perimenopausal Plantar Fasciitis
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 42
- 试验地点
- 1
- 主要终点
- Assessment of pain
研究概览
简要总结
The purpose of the study was to investigate the effect of phonophoresis versus iontophoresis on plantar fasciitis in perimenopausal women.
详细描述
Collagen plays a critical role in determining the tensile strength of connective tissue. During the perimenopausal transition, the overall quantity of collagen decreases; however, there is a relative increase in type I collagen compared to type III collagen. This shift contributes to increased tissue stiffness. Research indicates that estrogen has a protective effect on muscles and fascia, preventing fibrogenesis. Consequently, as estrogen levels decline during perimenopause, fibrogenic activity may increase. In addition, reduced estrogen levels are associated with enhanced elastin degradation, leading to diminished tissue elasticity and reduced recoil capacity.
This degradation of connective tissue is considered a primary cause of plantar fasciitis, which results from collagen breakdown in the plantar fascia at its origin-the calcaneal tuberosity of the heel-and surrounding fascial structures.
When plantar fasciitis develops in perimenopausal women, it can significantly disrupt daily activities. Many women experience fallen arches and severe irritation, with pain affecting functions such as standing, walking, climbing stairs, and working. This functional impairment can lead to emotional consequences, including depression.
Given these challenges, there is a pressing need to identify new, alternative, and cost-effective methods for managing and treating this condition. This study examined the effectiveness of phonophoresis and iontophoresis in treating plantar fasciitis in perimenopausal women. The findings aimed to contribute valuable knowledge to the field of physical therapy and offer practical solutions for women suffering from this condition.
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
- 50 Years 至 51 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •All participants were perimenopausal women who had been suffering from plantar fasciitis (PF) for at least one month.
- •Patients reported heel pain during the first step in the morning, while bearing weight, and after walking or running.
- •Diagnosis was confirmed using the Windlass test, Tarsal Tunnel test, and tenderness at the anterior medial heel.
- •Participants were aged between 50 and 51 years and experienced menstrual irregularities.
- •Their body mass index (BMI) was greater than 30 kg/m².
- •They had not received any medical treatment for plantar fascia pain or collagen supplements.
- •None of the participants were on hormonal therapy.
排除标准
- •Patients with a history of rheumatoid arthritis, diabetes mellitus, or hypertension.
- •Those diagnosed with neurological disorders.
- •Individuals who had undergone previous foot surgeries, experienced burns, or suffered severe foot trauma.
- •Participation in any other exercise training program during the study period.
- •History of skeletal deformities.
- •Presence of knee or ankle replacements.
- •Presence of ankle plates, screws, or nails.
- •Notable differences in lower limb length.
- •History of foot fractures that resulted in deformities.
- •Presence of infective foot conditions, dermatitis, or tumors.
- •Impaired circulation in the lower extremities.
- •Corticosteroid injection to the heel within the past year.
- •Congenital foot deformities.
研究组 & 干预措施
Phonophoresis
It consisted of 21 perimenopausal women. Each patient in this group received phonophoresis, 3 times per week, for 8 weeks.
干预措施: Phonophoresis (Other)
Iontophoresis
It consisted of 21 perimenopausal women. Each patient in this group received iontophoresis, 3 times per week, for 8 weeks.
干预措施: Iontophoresis (Other)
结局指标
主要结局
Assessment of pain
时间窗: 8 weeks
The Visual Analog Scale (VAS) was used to assess pain levels in each woman in both groups before and after the treatment program. Pain scores were determined by measuring the distance in millimeters on a 10-cm line between the "no pain" anchor and the patient's mark, yielding a score from 0 to 100. Higher scores indicated greater pain intensity. Recommended cut points were: no pain (0-4 mm), mild pain (5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm)
次要结局
- Measurement of the level of disability(8 weeks)
- Assessment of Dorsi flexion Range of Motion (ROM)(8 weeks)
研究者
Mereet Mokhles Zaref Farid
Principal Investigator
Cairo University