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临床试验/NCT07118397
NCT07118397进行中(未招募)不适用

Effect of Dry Needling Versus Kinesiology Taping in Patient With Plantar Fasciitis

University of Lahore1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年1月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
60
试验地点
1
主要终点
plantar fasciitis

研究概览

简要总结

A single-blinded randomized controlled trial was conducted at hamza hospital Lahore ,Lahore poly clinic over 9 months. A total of 60 participants aged 20-45 years with clinically diagnosed plantar fasciitis and identifiable myofascial trigger points were recruited using a non-probability purposive sampling technique. They were randomly assigned to two groups (n=30 each): Group A received dry needling with conventional physiotherapy once per week, while Group B received kinesiology taping with conventional physiotherapy twice per week. Both interventions were administered for 6 weeks. Outcome measures included the Visual Analogue Scale (VAS) for pain, Foot and Ankle Outcome Score (FAOS) for functional assessment, and SF-12 Health Survey for quality of life. Assessments were conducted at baseline, week 3, and week 6.

详细描述

A single-blinded randomized controlled trial will be conducted at hamza hospital Lahore ,Lahore poly clinic. Total sixty patients aged 20-45 years with clinically diagnosed plantar fasciitis and identifiable myofascial trigger points. Group A received dry needling with conventional physiotherapy once per week, while Group B received kinesiology taping with conventional physiotherapy twice per week. Both interventions were administered for 6 weeks. Outcome measures included the Visual Analogue Scale (VAS) for pain, Foot and Ankle Outcome Score (FAOS) for functional assessment, and SF-12 Health Survey for quality of life. Assessments were conducted at baseline, week 3, and week 6.

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)

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participants age group included was 20 - 45 years (Al-Boloushi, 2019)
  • •Both genders were selected
  • •The presence of MTrPs on plantar and calf muscles was assured (Al-Boloushi, 2019)
  • •Patients with plantar fasciitis from less than 1 month Eftekharsadat, 2016)

排除标准

  • •Participants who have had an MTP injection 3 months before treatment (Yasar, 2021)
  • •Participants who have had fractures, Inflammatory joint or systemic disease, skin ulcers and neuropathy (Cotchett, 2014)
  • •Participants who have needle phobia (Al-Boloushi, 2019)
  • •Participants with history of prior foot or plantar surgery were excluded (Jianing, 2025)

研究组 & 干预措施

group/kinesiology taping

Experimental

The taping was applied for over 12 hours daily and was reapplied twice a week for a total of six weeks

干预措施: kinesiology taping (Other)

group/dry needling

Experimental

Each dry needling session lasted for approximately 30 minutes. The total duration of the intervention was of 6 weeks with one session per week

干预措施: dry needling (Other)

结局指标

主要结局

plantar fasciitis

时间窗: changes from pre -interventions to 6th week

Plantar fasciitis is one of the most common causes of heel pain. It involves inflammation of a thick band of tissue that runs across the bottom of each foot and connects the heel bone to the toes, known as the plantar fascia

Pain Intensity

时间窗: changes from pre interventions to 6th week

Pain intensity will be measured using the Visual Analog Scale (VAS). The VAS is a continuous scale where participants indicate their pain level on a line ranging from 0 (no pain) to 10 (worst possible pain). The distance from the left end of the line to the participant's mark is measured in millimeters, providing a quantifiable score for pain intensity. A higher score reflects greater pain.

Functional Status

时间窗: changes from pre -interventions to 6th week

Functional status will be assessed using the Foot and Ankle Outcome Score (FAOS). The FAOS is a questionnaire designed to evaluate foot-related disability and pain, consisting of 13 items distributed across three domains: pain, disability, and activity limitation. Each item is rated from 0 (no problem) to 4 (severe problem). Scores for each domain are summed and averaged, with higher scores indicating worse functional status

Quality of Life(SF-12 )

时间窗: changes form pre-interventions to 6th week

The SF-12 Health Survey will be used to assess quality of life. This tool evaluates physical and mental health outcomes, with scores reflecting overall well-being and daily functioning before and after treatment. The SF-12 provides a comprehensive measure of the impact of interventions on patients' quality of life. Scores above 50 indicate a better-than-average health-related quality of life, while scores below 50 suggest below-average health.

次要结局

未报告次要终点

研究者

发起方
University of Lahore
申办方类型
Other
责任方
Principal Investigator
主要研究者

Anam Ashraf

physical therapist

University of Lahore

研究点 (1)

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