跳至主要内容
临床试验/NCT04941469
NCT04941469已完成不适用

Effectiveness of Specifically Optimized Off-the-counter Foot Orthosis for the Management of Mechanical Foot Pains in the Subtle Cavus Foot Type: A Pilot-controlled Study

Tan Tock Seng Hospital2 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2021年10月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
29
试验地点
2
主要终点
The Change in Foot Function Index (FFI) total score from baseline at Week 12

研究概览

简要总结

As off-the-counter foot orthoses are readily available and have an economic advantage, they are increasingly being used by healthcare professionals to treat mechanical foot pains in place of custom foot orthosis. However, there is a lack of available evidence to determine if a plain off-the-counter foot orthosis that aims to contours to the foot or a specifically optimized off-the-counter foot orthosis utilizing the type of orthotic design proposed by Abbasian and Pomeroy is more effective in the management of mechanical foot pains in the Subtle Cavus foot type.

This study proposal seeks to fill the gap in this area.

Primary Aim:

To investigate the effectiveness of specifically optimized off-the-counter foot orthosis designed for the Subtle Cavus foot type in improving patient reported outcomes in patients with mechanical foot pains when compared to plain off-the-counter foot orthosis.

Primary Null Hypothesis:

There is no difference in pain and functional scores reported by patients between specifically optimized off-the-counter foot orthosis and plain off-the-counter foot orthosis in patients with mechanical foot pains at four, eight and twelve weeks of intervention.

In our study, the Subtle Cavus foot refers to the flexible idiopathic forefoot-driven Pes Cavus that can be clinically recognised with a positive "Peek a Boo" sign, inverted hindfoot position in weight bearing stance and Positive Coleman Block Test as reported by Manoli and Graham in 2005.

Also, for our study, mechanical foot pains are limited to clinically diagnosed Plantar Fasciitis, Achilles Tendinopathy, Peroneal Strain or Metatarsalgia:

Plantar Fasciitis is clinically diagnosed using the following history and physical examination findings:

  • Plantar medial heel pain /or pain along the plantar fascia: most noticeable with initial steps after a period of inactivity but also worse following prolonged weight bearing
  • Heel pain /or pain along the plantar fascia precipitated by a recent increase in weightbearing activity
  • Pain with palpation of the proximal insertion of the plantar fascia /or along the band of plantar fascia structure

Achilles Tendinopathy is clinically diagnosed using the following history and physical examination findings:

Midportion Achilles Tendinopathy:

  • Self-reported localized pain and perceived stiffness in the Achilles tendon following a period of inactivity (eg, sleep, prolonged sitting) lessen with an acute bout of activity and may increase after the activity.
  • Symptoms are frequently accompanied by Achilles tendon tenderness.
  • Pain located 2 to 6 cm proximal to the Achilles tendon insertion that began gradually and pain with palpation of the midportion of the tendon to diagnose midportion Achilles tendinopathy

Insertional Achilles Tendinopathy:

  • Self-reported pain that is aggravated by activity and stiffness that is associated with prolonged periods of rest.
  • Pain and tenderness with palpation within the distal 2 cm of the Achilles tendon.
  • Redness and swelling over area of Achilles Tendon insertion over posterior heel

Peroneal Strain is clinically diagnosed using the following history and physical examination findings:

  • Pain and swelling posterior to the lateral malleolus
  • Pain with active eversion and dorsiflexion against resistance
  • May have a history of chronic lateral ankle pain and instability
  • Pain and tenderness with palpation along the course of the peroneal tendons

Metatarsalgia is clinically diagnosed using the following history and physical examination findings:

  • Self-reported pain during the propulsive phase of gait. The pain is localized underneath the prominent metatarsal heads
  • The plantar soft tissue can be swollen and inflamed.
  • Presence of hyperkeratosis over tender areas may be present
  • Pain and tenderness with palpation of plantar metatarsophalangeal joints

Secondary Aim:

To investigate the effectiveness of specifically optimized off-the-counter foot orthosis designed for the Subtle Cavus foot type in improving patient reported outcomes in patients with mechanical foot pains pre- and post-intervention.

Secondary Null Hypothesis:

There is no difference in pain and functional scores reported by patients after introduction of specifically optimized off-the counter foot orthosis pre- and post-intervention at initial to four, initial to eight and initial to twelve weeks of intervention.

详细描述

Study Design:

This is a Pilot Randomized Controlled Trial designed to compare the effectiveness of specifically optimized off-the-counter foot orthosis versus plain off-the-counter foot orthosis in managing mechanical foot pains in the Subtle Cavus foot type. (See Figure 3).

  • Subjects recruited will be randomly assigned to either the plain off-the-counter foot orthosis group (Control Group) or the specifically optimized off-the-counter foot orthosis group (Intervention Group) based on a pre-specified randomization list during the Screening Visit.
  • Randomization was performed using the Randomized Permuted Block Randomization method with blocks of six.
  • For participants with bilateral mechanical foot pains, the more symptomatic side will be used as the reference for collection of participants reported outcome measures throughout the study.
  • There will be an intervention period of 12 weeks, which is a common therapy window for the associated symptoms of mechanical foot pains.
  • All other standard of care Podiatry management will be implemented for all subjects in the two groups throughout the study period.
  • Standard Podiatry management with stretching exercise regime refers to the following protocols with official department stretching and strengthening brochure provided for all subjects:

Towel Stretch (To be introduced at Study Visit 1 (Week 0)):

Sit down and extend both legs Pass a towel around the top of your foot Slowly pull the towel towards your body Hold each stretch for a period of 20 seconds Switch sides and repeat Repeat the stretch 10 times on both sides for each set Perform 2 sets a day

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
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 21-80 years old
  • Able to provide informed consent
  • Clinically diagnosed mechanical foot pains limited to Plantar Fasciitis, Achilles Tendinopathy, Peroneal Strain or Metatarsalgia.
  • Clinically recognized Subtle Cavus foot type
  • Positive "Peek a boo" sign
  • Hind foot / Rearfoot / Heel in varus position in weight bearing stance
  • Positive Coleman Block Test (rearfoot inversion correctable)
  • Able to comply with all study procedures

排除标准

  • Age < 21 Years old
  • History of surgery in the lower limb
  • History of trauma or falls prior to onset of symptoms or after
  • Pregnancy or breastfeeding women
  • Pes Planus foot type
  • Rigid Pes Cavus (Negative Coleman Block Test)
  • Nervous system problems (e.g., stroke, dementia, seizures)
  • Peripheral vascular pathology
  • Acute infection
  • Rheumatic joint disease
  • Inability to comply to wearing appropriate footwear and foot orthosis
  • Lack of willingness to return for follow-up
  • Musculoskeletal pathology other than Plantar Fasciitis, Achilles Tendinopathy, Peroneal Strain or Metatarsalgia

结局指标

主要结局

The Change in Foot Function Index (FFI) total score from baseline at Week 12

时间窗: Study Visit 4 (Week 12) vs Study Visit 1 (Week 0)

* The FFI is a self-reported measure of pain, function, and activity level associated with foot dysfunction consisting of 23 items divided into 3 sub-scales. The scores range from 0 to 10, with the higher scores indicating more disability. * The FFI has been validated and is recommended as a reliable measurement scale for use in foot orthotic interventions study. * The evaluation of the study device efficacy will be conducted with the main outcome measure, the FFI before and after intervention.

The Foot Function Index (FFI) total score

时间窗: Study Visit 4 (Week 12)

* The FFI is a self-reported measure of pain, function, and activity level associated with foot dysfunction consisting of 23 items divided into 3 sub-scales. The scores range from 0 to 10, with the higher scores indicating more disability. * The FFI has been validated and is recommended as a reliable measurement scale for use in foot orthotic interventions study. * The evaluation of the study device efficacy will be conducted with the main outcome measure, the FFI between the control and treatment groups.

The Change in Foot Function Index (FFI) total score from baseline at Week 4

时间窗: Study Visit 2 (Week 4) vs Study Visit 1 (Week 0)

* The FFI is a self-reported measure of pain, function, and activity level associated with foot dysfunction consisting of 23 items divided into 3 sub-scales. The scores range from 0 to 10, with the higher scores indicating more disability. * The FFI has been validated and is recommended as a reliable measurement scale for use in foot orthotic interventions study. * The evaluation of the study device efficacy will be conducted with the main outcome measure, the FFI before and after intervention.

The Change in Foot Function Index (FFI) total score from baseline at Week 8

时间窗: Study Visit 3 (Week 8) vs Study Visit 1 (Week 0)

* The FFI is a self-reported measure of pain, function, and activity level associated with foot dysfunction consisting of 23 items divided into 3 sub-scales. The scores range from 0 to 10, with the higher scores indicating more disability. * The FFI has been validated and is recommended as a reliable measurement scale for use in foot orthotic interventions study. * The evaluation of the study device efficacy will be conducted with the main outcome measure, the FFI before and after intervention.

次要结局

  • 100mm Visual Analogue Scale (VAS) with the end-points "no pain" and "worst pain possible"(Study Visit 4 (Week 12))
  • The FFI sub-scale scores in the domain of activity limitation(Study Visit 4 (Week 12))
  • The Change in FFI sub-scale scores in the domain of pain from baseline at Week 8(Study Visit 3 (Week 8) vs Study Visit 1 (Week 0))
  • The Change in FFI sub-scale scores in the domain of disability from baseline at Week 8(Study Visit 3 (Week 8) vs Study Visit 1 (Week 0))
  • The Change in FFI sub-scale scores in the domain of disability from baseline at Week 12(Study Visit 4 (Week 12) vs Study Visit 1 (Week 0))
  • The FFI sub-scale scores in the domain of pain(Study Visit 4 (Week 12))
  • The Change in FFI sub-scale scores in the domain of pain from baseline at Week 4(Study Visit 2 (Week 4) vs Study Visit 1 (Week 0))
  • The Change in FFI sub-scale scores in the domain of pain from baseline at Week 12(Study Visit 4 (Week 12) vs Study Visit 1 (Week 0))
  • The FFI sub-scale scores in the domain of disability(Study Visit 4 (Week 12))
  • The Change in FFI sub-scale scores in the domain of disability from baseline at Week 4(Study Visit 2 (Week 4) vs Study Visit 1 (Week 0))
  • The Change in FFI sub-scale scores in the domain of activity limitation from baseline at Week 4(Study Visit 2 (Week 4) vs Study Visit 1 (Week 0))
  • The Change in FFI sub-scale scores in the domain of activity limitation from baseline at Week 8(Study Visit 4 (Week 12) vs Study Visit 1 (Week 0))

研究者

发起方
Tan Tock Seng Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ng Chuan Guan

Senior Podiatrist

Tan Tock Seng Hospital

研究点 (2)

Loading locations...

相似试验

Effectiveness of Specifically Optimized... | 临床试验