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临床试验/NCT05258188
NCT05258188已完成不适用

Study Comparing the Effectiveness of Ergon Instruments-Assisted Soft Tissue Mobilization Techniques With Compressive Myofascial Release for Plantar Fasciitis: A Randomised Clinical Trial

Riphah International University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Range of Motion

研究概览

简要总结

The objective of this study is to investigate the effects of Virtual Reality and Motor Imagery along with Routine Physical Therapy in motor function and balance in patients with Parkinson disease.

详细描述

This randomized control trial is the single blinded, single centered study. Standard Protocol Items: Recommendations for Interventional Trials guidelines are used as study protocol. Sixty three patients of Parkinson Disease (Modified Hoehn and Yahr stages I-III) will randomly allocate into three groups.

Group A will be given a 60 min session of Virtual Reality along with Routine Physical Therapy.

Group B will be given a 60 min session of Motor Imagery along with Routine Physical Therapy.

Group C will be given a 40 min session of Routine Physical Therapy and after a short period of rest,20 min for walking and cycling.

These treatment sessions will be given to each group at every alternative day (3 days per week) for 12 weeks.

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
Single (Outcomes Assessor)

盲法说明

Our study will be single-blinded, outcome assessor-blinded. The assessor will be blinded to avoid being biased during the outcome assessment.

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Inability to achieve 20 degrees of active dorsiflexion,
  • •Heel pain,
  • •Mid foot pain,
  • •Heal swelling,
  • •Mid foot swelling,
  • •Achilles' tendon tightness diagnosed on the base of Windlass test

排除标准

  • •Recent foot injury,
  • •Fracture,
  • •Infections,
  • •Surgical procedures,
  • •Tendon injury,
  • •Hypermobility,
  • •Neuromuscular disorders,
  • •Impaired sensation,
  • •Open sores,
  • •Skin disease,
  • •Active deep vein thrombosis or thrombophlebitis,
  • •Varicose veins,
  • •Burn scars

研究组 & 干预措施

Instrument-assisted Soft Tissue Mobilization

Experimental
  1. Warm-up will be performed for 10 to 15 minutes by light jogging, elliptical machine, stationary cycle or an upper body ergometer
  2. Instrument-assisted Soft Tissue Mobilization , will be applied at 30 to 60 degrees angle for 40 to 120 seconds
  3. Stretching, for 30 seconds (3 rep)
  4. Strengthening exercises, high repetitions with low intensity exercise
  5. Cryotherapy for 10 to 20 min

干预措施: Instrument-assisted Soft Tissue Mobilization (Other)

Compressive Myofascial Release Technique

Experimental

Compressive myofascial release technique will be applied 5 minutes, after a warmup of 10 to 15 minutes.

干预措施: Compressive Myofascial Release Technique (Other)

结局指标

主要结局

Range of Motion

时间窗: 12th Week

Goniometer has been the most widely used tool for measuring joint range of motion. To ensure reliable measurement, standardized, specific positions and landmarks are used to measure each joint movement.

Visual Analogue Scale

时间窗: 12th Week

The Visual Analog Scale is a 10 cm line with anchor statements on the left, no pain and on the right, extreme pain.

Foot and Ankle Disability Index

时间窗: 12th Week

The Foot and Ankle Disability Index has 26 items. Each item is scored from 0; unable to do, to 4; no difficulty at all. The Foot and Ankle Disability Index has a total point value of 104 points.

Foot and Ankle Ability Measure

时间窗: 12th Week

The Foot and Ankle Ability Measure (FAAM) is a self-report outcome instrument/questionaire developed to assess physical function for individuals with foot and ankle related impairments. 8-item Sports Subscale. Each item is scored on a 5-point Likert scale (4 to 0) from 'no difficulty at all' to 'unable to do'. Item score totals, which range from 0 to 84 for the ADL subscale and 0 to 32 for the Sports subscale, were transformed to percentage scores. Higher scores represent higher levels of function for each subscale, with 100% representing no dysfunction.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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