性少数群体中的少数群体压力、应激负荷与药物和酒精使用之间的关联:酷儿健康研究——纵向可行性评估方案

Associations Among Minority Stress, Allostatic Load, and Drug and Alcohol Use in Sexual Minorities: Protocol for the Queer Health Study-a Longitudinal Feasibility Evaluation.

作者信息

Smith Nathan Grant, Chen Tzuan A, Juster Robert-Paul, Obasi Ezemenari M, Crocker Jacob S

机构信息

Department of Psychological, Health, and Learning Sciences, College of Education, University of Houston, Houston, TX, United States.

Department of Psychiatry & Addiction, Université de Montréal, Montreal, QC, Canada.

出版信息

JMIR Res Protoc. 2025 Jun 27;14:e73070. doi: 10.2196/73070.

Abstract

BACKGROUND

Substance use rates among sexual minorities are disproportionately greater than that of their heterosexual counterparts. Minority stress theory posits that one explanation for disproportionate substance use in sexual minority populations is a result of increased social stress associated with holding a minoritized identity. This minority stress has been linked to a myriad of negative mental health outcomes, including alcohol and drug use. In addition, emerging research has begun to demonstrate links between minority stress and stress physiology dysregulation. While animal and human models have demonstrated links between stress physiology dysregulation and substance use outcomes, to date, no studies have examined the role that stress physiology plays within a minority stress framework in predicting substance use among sexual minorities. The Queer Health Study was designed to explore the longitudinal links among minority stress, stress physiology (specifically, allostatic load, the cumulative "wear and tear" on the body and brain as a result of chronic stress), and substance use.

OBJECTIVE

This study aims to assess the feasibility of collecting longitudinal data to explore the temporal links between minority stress processes, allostatic load, and drug and alcohol use, as well as to obtain estimates of effect size to determine the appropriate sample size necessary to conduct a fully powered longitudinal study.

METHODS

This feasibility study is a 3-wave longitudinal design consisting of a self-report survey, researcher-assisted Timeline Followback to assess for drug and alcohol use, and blood and anthropometric data collection to measure allostatic load at each of the time points. A total of 40 ethnically and racially diverse sexual minority adult participants (aged 18-60 years) will be enrolled.

RESULTS

The study received University of Houston institutional review board approval on July 31, 2023 (STUDY00004277). Recruitment began in June 2024. As of February 2025, the initial sample of 46 participants completed the time 1 visit, and time 2 visits are ongoing. We estimate that all study activities will be completed by July 2025.

CONCLUSIONS

Results can inform the development of targeted prevention and treatment interventions. In addition, this research will provide an innovative framework for exploring diverse risk and resilience factors impacting addiction in this at-risk population. Ultimately, results have important implications for public health and have the potential to reduce the many dire economic and health consequences of drug use and addiction.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/73070.

摘要

背景

性少数群体中的物质使用发生率远高于异性恋群体。少数群体压力理论认为,性少数群体中物质使用比例过高的一个原因是,持有少数群体身份会带来更多社会压力。这种少数群体压力与一系列负面心理健康结果有关,包括酒精和药物使用。此外,新出现的研究已开始证明少数群体压力与应激生理调节异常之间存在联系。虽然动物和人类模型已证明应激生理调节异常与物质使用结果之间存在联系,但迄今为止,尚无研究探讨应激生理在少数群体压力框架中对预测性少数群体物质使用所起的作用。酷儿健康研究旨在探索少数群体压力、应激生理(具体而言,是负荷应激,即慢性应激对身体和大脑造成的累积“损耗”)和物质使用之间的纵向联系。

目的

本研究旨在评估收集纵向数据以探索少数群体压力过程、负荷应激与药物和酒精使用之间的时间联系的可行性,并获得效应量估计值,以确定进行一项有充分效力的纵向研究所需的合适样本量。

方法

这项可行性研究采用三波纵向设计,包括一份自我报告调查问卷、研究人员协助的时间线回溯法以评估药物和酒精使用情况,以及在每个时间点收集血液和人体测量数据以测量负荷应激。总共将招募40名年龄在18至60岁之间、种族和民族多样的性少数成年参与者。

结果

该研究于2023年7月31日获得休斯顿大学机构审查委员会批准(研究编号:STUDY00004277)。招募工作于2024年6月开始。截至2025年2月,最初的46名参与者样本完成了第1次访视,第2次访视正在进行中。我们估计所有研究活动将于2025年7月完成。

结论

研究结果可为制定有针对性的预防和治疗干预措施提供参考。此外,本研究将提供一个创新框架,以探索影响这一高危人群成瘾的各种风险和复原力因素。最终,研究结果对公共卫生具有重要意义,并有潜力减少药物使用和成瘾造成的诸多严重经济和健康后果。

国际注册报告识别码(IRRID):DERR1-10.2196/73070。

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