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临床试验/NCT07576582
NCT07576582招募中不适用

The Effect of Peloid Therapy on Pain and Functional Outcomes in Patients With Temporomandibular Joint Dysfunction

Uşak University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年4月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
1

研究概览

简要总结

This prospective, single-group clinical study will evaluate whether local peloid therapy improves pain and jaw function in adults with temporomandibular joint dysfunction. Participants will receive peloid therapy applied to the temporomandibular joint region and masticatory muscles for 20 minutes per session, 5 days per week, for 2 weeks. Pain and functional outcomes will be measured at baseline and at the end of treatment using validated clinical scales, including the Jaw Functional Limitation Scale-8, visual analog scale pain scores, Fonseca index, maximum mouth opening, and secondary otalgia assessment.

详细描述

Temporomandibular joint dysfunction is associated with pain, impaired chewing, restricted jaw function, and, in some patients, referred otalgia. Conservative treatment options are commonly used as first-line management, but the clinical evidence for some physical therapy modalities remains limited.

Peloid therapy is a local thermotherapeutic intervention used in balneotherapy and physical medicine. It may provide analgesic and muscle-relaxing effects through superficial heat and local tissue responses. However, prospective data evaluating its clinical effect in temporomandibular joint dysfunction are limited.

This study is designed to assess changes in jaw-related functional limitation and pain after a standardized 2-week course of local peloid therapy in adults diagnosed with temporomandibular joint dysfunction. Functional status, pain intensity, mouth opening, symptom severity, and secondary otalgia will be assessed before and after treatment using standardized clinical measures.

The study may provide additional evidence on the role of peloid therapy as a conservative supportive treatment option for temporomandibular joint dysfunction.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years
  • Diagnosis of temporomandibular joint dysfunction based on DC/TMD criteria
  • Presence of TMJ-related pain for at least 4 weeks
  • Baseline pain intensity ≥3 on a 0-10 visual analog scale
  • Ability to provide written informed consent

排除标准

  • History of temporomandibular joint trauma, tumor, active infection, or acute inflammation
  • Previous temporomandibular joint surgery
  • Presence of systemic inflammatory rheumatologic disease
  • Pregnancy
  • Open wound, active dermatitis, or skin condition preventing peloid application at the treatment site
  • Injection therapy (e.g., botulinum toxin) or regular physical therapy for TMJ within the past 3 months
  • Any clinical or behavioral condition that may interfere with study compliance

研究组 & 干预措施

Peloid Therapy

Experimental

干预措施: Local Peloid Therapy (Other)

研究者

发起方
Uşak University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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Peloid Therapy in Temporomandibular Joint Dysfunction | 临床试验