跳至主要内容
临床试验/NCT06353789
NCT06353789招募中不适用

Understanding the Role of Adolescent Dysmenorrhoea as a Risk Factor for the Transition to Chronic Pain: Clinical Cohort Study

University of Oxford1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2024年6月4日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
132
试验地点
1
主要终点
Quantitative Sensory Testing (QST)

研究概览

简要总结

This study aims to understand whether changes in a variety of body systems which are seen in adult women with period pain are also seen in adolescents in the first few years of having periods. This information will help to understand 1) how quickly any changes occur, informing clinical practice, and 2) how period pain might lead to other types of chronic pain, potentially allowing development of preventative strategies.

详细描述

Chronic pain is defined as pain that lasts for more than 3 months. It is really common, affecting up to 30% of people worldwide with impacts on all areas of life. Chronic pain is difficult to treat once it has developed. Therefore, understanding which people might be at risk of developing chronic pain and protecting them from it starting, would be a really positive step forward.

It is known that women are more likely to develop almost all types of chronic pain than men. This sex difference in chronic pain starts to be seen after puberty, suggesting that changes happening at this time may be contributing to this increased risk. One important change that happens at this time is periods starting. Despite periods often being very painful, period pain has traditionally been dismissed as "normal" and something girls must learn to live with. However, in adult women with period pain many differences are seen across a range of body systems when compared to women without period pain. These include increased sensitivity to pain; increased sensitivity of the bladder, bowel and womb; altered brain structure and function; and altered responses to stress. Similar changes to those seen with period pain can be seen in other chronic pain conditions. It is not known whether these changes are caused by repeated or continuous pain or if they are part of the reason why chronic pain develops, or a combination of both.

The RoADPain Clinical Study aims to see whether the differences in other body systems described above in adult women with period pain are also seen in girls in the first few years of having periods. The investigators will combine detailed questionnaire data with tests of the function of a variety of systems (including nerve function, stress response and brain imaging). No study treatment or intervention will be given. It is envisaged that this information will help to understand 1) how quickly any changes occur, informing clinical practice, and 2) how period pain might lead to other types of chronic pain, potentially allowing development of preventative strategies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
11 Years 至 20 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Participant (or parent/guardian of participant) is willing and able to give informed consent for participation in the study.
  • Female or assigned female at birth.
  • aged 11 - 20 years.
  • At least 6 periods per year since menarche.
  • During the study data collection period will be within one of the following time intervals since menarche:
  • 12 - 15 months
  • 36 - 39 months
  • 60 - 63 months
  • Reports either period pain or no pain with periods and scores appropriately on NRS (period pain: ≥4/10; no period pain: ≤3/10).
  • Not using hormonal therapies (i.e. contraceptives) currently and has not used previously.
  • Reasonably fluent in English.

排除标准

  • Current or previous chronic pain condition other than dysmenorrhoea, including migraine.
  • Pregnant or breast-feeding.
  • Previous cancer diagnosis.
  • Contraindication to MRI

结局指标

主要结局

Quantitative Sensory Testing (QST)

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

QST of the left hand according to the German Neuropathic Pain Network Protocol plus an auditory stimulus.

Heart rate (HR)

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Assessed over a 20 minute period at rest.

Change in heart rate

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Assessed at rest immediately before the CPM paradigm described below and then again immediately after. The ischaemic pain stimulus used as the conditioning stimulus in this paradigm is the most noxious component of the physiological testing paradigms used in this study and therefore the most likely to generate a stress response. The change will be reported as HR(before) - HR(after).

Bladder sensitivity to filling

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Assessed with standardised non-invasive bladder filling paradigm, measured as time to verbal reports of different sensations of bladder fullness (first sensation, first urge) and then need to void (maximum tolerance) after drinking 600 ml water. Subjects will be categorised into those with bladder sensitivity compared to published norms for similar age adolescents and those with normal bladder sensation.

Pain Catastrophising: Pain Catastrophising Scale (PCS) (Sullivan)

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Measured with the Pain Catastrophising Scale (Sullivan). Scores range from 0 - 52 with high scores representing higher levels of pain catastrophising. Although three sub scales exist they will not be assessed for the purposes of these main analyses.

Volume voided at maximum tolerance

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Assessed with standardised non-invasive bladder filling paradigm described in outcome 4. The volume of urine voided when maximum tolerance is reached will be measured in mls.

Area under the curve (AUC) of single day salivary cortisol profile

时间窗: days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.

Saliva will be collected at home at the specified times allowing a daily AUC of salivary cortisol for each subject to be calculated. Collection times: waking; 30-45 minutes after waking; before lunch; before dinner; bedtime.

次要结局

  • fMRI scan(days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.)
  • Change of pressure pain threshold (PPT)(days 1-3 (menstrual phase) and days 10-12 (follicular phase) of the menstrual cycle.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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