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临床试验/NCT07735520
NCT07735520尚未招募不适用

Evaluating the Feasibility and Acceptability of Expectation-optimized Open-label Placebo as an Adjuvant Treatment for Chronic Pain

University of Maryland, Baltimore0 个研究点目标入组 57 人开始时间: 2027年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
57
主要终点
Enrollment rate

研究概览

简要总结

The primary objective is to determine the feasibility of delivering OLP-EXP, EXP only, and OLP only over 6 weeks to adults with chronic TMD. The trial will be considered feasible for progression planning when the 6-week retention rate is at least 80% in each arm and average OLP pill adherence is at least 80% of prescribed days in each OLP arm.

Primary hypothesis: Each intervention arm will meet the prespecified 6-week retention benchmark, and each OLP arm will meet the prespecified pill-adherence benchmark.

The secondary objectives are:

  1. To evaluate acceptability of each intervention using the TFA measurement and semi-structured interviews.
  2. To assess the feasibility of collecting daily EMA, continuous actigraphy, weekly questionnaires, and 3-, 6-, and 12-month follow-up assessments.
  3. To identify intervention barriers, facilitators, perceived benefits, burden, ethical concerns, and recommendations for a future fully powered efficacy trial.
  4. To estimate variability, missingness, and measure reliability needed to select outcomes and design a future trial.

详细描述

Pain lasting for more than 3 months becomes chronic, and is prevalent across the global population. Among chronic pain conditions, temporomandibular disorders (TMD), a common orofacial pain condition affecting 9 to 30% of the general population, have attracted the attention of clinical providers and researchers. The high incidence and disastrous consequences of TMD underscore the need for effective and safe treatments.

Clinical and mechanistic research has shown substantial placebo responses in pain trials, highlighting the great potential to harness placebo mechanisms in clinical care. For example, a meta-analysis estimated that placebo responses could account for up to 66% of observed improvement in migraine-related outcomes.8 In one efficacy and safety trial of an intravenously eptinezumab, as much as 74% of the apparent benefit was attributed to placebo responses.

In ethically translating placebo mechanisms, open-label placebo (OLP) offers an adjuvant to current pharmacological and psychological treatments for chronic pain. OLP refers to the transparent, honest administration of placebos. Studies have found that people can still experience improvements in symptoms even after receiving OLP.

Previous RCT has demonstrated efficacy of EXPECT in a pilot clinical trial showing a reduction in the length of hospital stay after cardiac surgery. Moreover, participants who received EXPECT showed greater improvements in disability, and reduced pro-inflammatory cytokine concentrations compared to those in the treatment as usual group.

The investigators aim to develop an expectation-optimized OLP intervention (OLP-EXP) that could potentially maximize OLP effects and yield larger improvement in managing chronic pain, and an EXP only intervention that delivers expectations induced analgesia without the negative connotations of "placebo".

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

盲法说明

In this open-label placebo trial, both the experimenters and participants will be aware of the arms assignment. The outcome assessor will be blinded about the group assignment.

入排标准

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

入选标准

  • English speaking (written and spoken)
  • Age between 18 and 65 years
  • Confirmed TMD for more than 3 months
  • Grade II or above on the Graded Chronic Pain Scale

排除标准

  • Personal (or family first degree) history of mania, schizophrenia, or other psychoses
  • Severe psychiatric conditions require medication (e.g. schizophrenia, bipolar disorders, autism) or hospitalization within the last 3 years.
  • Lifetime alcohol/drug dependence and alcohol/drug abuse in past one year
  • Pregnancy/Breastfeeding
  • Currently participating in another clinical trial

结局指标

主要结局

Enrollment rate

时间窗: At the enrollment

Enrollment rate: the proportion (%) of recruited participants who enrolled in the study.

Retention rate

时间窗: End of week 6

Retention rate: the proportion (%) of enrolled participants who finished the study

Daily survey completion rate

时间窗: End of week 6

Module rate: the proportion (%) of completed daily surveys sent through DockTales and REDCap-based surveys.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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