Manson Unit, Médecins Sans Frontières, London, UK
Department of Sociology, University of Sussex, Brighton, UK.
BMJ Open. 2021 Sep 6;11(9):e043954. doi: 10.1136/bmjopen-2020-043954.
People living with multidrug-resistant tuberculosis currently have few options for effective treatment and cure. Regimens that are available are toxic, may involve injections and take up to 2 years to complete treatment, with success rates as low as 50%. The TB-PRACTECAL trial is evaluating shorter, more tolerable regimens of oral drugs; we detail the substudy within this trial, PRACTECAL-PRO, which aims to evaluate patient experiences and perspectives on treatment, to understand outcomes more fully.
We are conducting a mixed-methods evaluation within both investigational and standard of care arms within the TB-PRACTECAL trial, using sequential quality of life (QoL) surveys and in-depth interviews. Data collection involves the Short Form 12 (SF-12) and St George's Respiratory Questionnaire (SGRQ), collected at up to four fixed timepoints, from baseline, to up to 12 months later. Healthy volunteers will be surveyed to establish locally relevant controls. We will also purposively sample participants for qualitative data collection and analysis, to provide rich explanation of QoL scores. The study will be implemented in all six TB-PRACTECAL study sites in Uzbekistan, South Africa and Belarus. QoL surveys will be scored and analysed according to SF-12 and SGRQ developers' manuals. Differences between scores at baseline and later timepoints will be evaluated as well as graphical exploration of group score trajectories of investigational and standard of care arms.
Ethics approval was obtained from the Médecins Sans Frontières Ethics Review Board. Local ethics approval has been obtained in Uzbekistan, Belarus and South Africa. Results of the substudy will be shared with local health authorities, the WHO and submitted for publication in a peer-reviewed journal.
NCT03942354; Pre-results.
目前,耐多药结核病患者的有效治疗和治愈选择有限。现有的治疗方案毒性大,可能需要注射,且治疗时间长达 2 年,成功率仅为 50%。TB-PRACTECAL 试验正在评估更短、更耐受的口服药物治疗方案;我们详细介绍了该试验中的子研究 PRACTECAL-PRO,旨在评估患者对治疗的体验和看法,以更全面地了解治疗结果。
我们正在 TB-PRACTECAL 试验的研究和标准治疗组内开展一项混合方法评估,使用顺序性生活质量 (QoL) 调查和深入访谈。数据收集包括使用短期 12 项健康调查 (SF-12) 和圣乔治呼吸问卷 (SGRQ),在多达四个固定时间点进行测量,从基线到 12 个月后。健康志愿者将接受调查以建立当地相关的对照。我们还将有针对性地对参与者进行定性数据收集和分析,以充分解释 QoL 评分。该研究将在乌兹别克斯坦、南非和白俄罗斯的所有六个 TB-PRACTECAL 研究地点实施。QoL 调查将根据 SF-12 和 SGRQ 开发者手册进行评分和分析。将评估基线和以后时间点之间的评分差异,以及对研究和标准治疗组的组评分轨迹进行图形探索。
该研究已获得无国界医生伦理审查委员会的伦理批准。乌兹别克斯坦、白俄罗斯和南非已获得当地伦理批准。子研究的结果将与当地卫生当局、世界卫生组织共享,并提交给同行评议期刊发表。
NCT03942354;预结果。