ACTRN12621000645853招募中未知
Efficacy of footwear, foot orthoses and exercise for the conservative management of painful hallux valgus in women: a randomised pilot and feasibility trial
a Trobe University0 个研究点目标入组 28 人开始时间: 2021年5月28日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 28
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 40 Years 至 o limit(—)
- 性别
- Female
入选标准
- •To be eligible for inclusion, participants must:
- •(i) be aged >=40 years;
- •(ii) be female;
- •(iii) have pain in the toe joint/s (i.e. first metatarsophalangeal or interphalangeal) for at least 12 weeks;
- •(iv) have pain in the toe joint/s (i.e. first metatarsophalangeal or interphalangeal) rated at least 3 out of 10 on a numerical rating scale;
- •(v) be able to walk household distances (more than 50 m) without the aid of a walker, crutches or cane;
- •(vi) be capable of understanding the English language in verbal and written form, and;
- •(vii) have at least moderate hallux valgus on one or both feet, defined as a score of 2 or more on the validated Manchester scale, a tool containing four standardised photographs of varying degrees of hallux valgus deformity.
排除标准
- •Participants will not be eligible for inclusion if they have:
- •(i) had surgical treatment for hallux valgus on either foot;
- •(ii) had a lower limb or partial foot amputation;
- •(iii) have an inflammatory rheumatological condition such as gout, rheumatoid arthritis, psoriatic arthritis, axial spondyloarthropathy or connective tissue disease, (iv) have a neurological disease which interferes with walking (e.g. Parkinson’s disease);
- •(v) have worn arch-contouring foot orthoses in the past 12 weeks (although flat insoles will be permitted);
- •(vi) have been performing foot exercises (stretching, mobilisation or strengthening) in the past 12 weeks, or;
- •(vii) have an injury of lower limb(s) or back that may interfere with reaching their feet.
研究者
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