Evaluation of a Health Literacy Intervention on Patients Suffering From Hypertension in Primary Care
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 255
- 主要终点
- Proportion of patients with a home-measured blood pressure within the therapeutic target
研究概览
简要总结
Hypertension affects 30% of the French population, but only 25% of hypertensive patients meet therapeutic targets, largely due to a limited adherence to lifestyle and medication guidelines (34%). Improving adherence is crucial to better blood pressure control and preventing complications. Health literacy (HL), defined by Sørensen as the ability to access, evaluate, and use health information for decision-making, has been proved associated with better adherence. Various tools, such as the "Teach-Back" method, can enhance HL but are underutilized in France due to lack of awareness and training. The objective of this study is to evaluate the effectiveness of a multi-component intervention aimed at increasing the health literacy of patients suffering from hypertension, in achieving the target blood pressure goal three months after the start of the intervention in poorly controlled hypertensive patients. The intervention will include tools (such as communication techniques) enabling physicians to enhance the health literacy of their patients.
详细描述
The study comprises two phases. The first phase will involve a qualitative analysis, during which semi-structured interviews will be conducted to understand the constraints, expectations, and needs of both physicians and patients for the intervention. After this phase, an intervention following the Health Literacy Intervention Model will be constructed, through a consensus method .
The second phase of the study will be a mixed-method evaluation of the intervention's effectiveness. Initially, a cluster-randomized trial will be conducted. Thirty-six physicians will participate and randomized into either the control group or the intervention group. Each physician will recruit approximately 5 patients. Patients will undergo a pre-inclusion visit, an inclusion visit, and then three follow-up visits (at 3 and 6 months). Finally, all participating physicians and a subsample of 30 patients will take part in the qualitative study to assess the perceived effectiveness of the intervention.
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
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Phase 1: Co-construction of the Intervention
- •o In this phase, physicians and patient representatives from patient associations or recruited through physicians will be enrolled.
- •Phase 2: Evaluation of the Intervention's Effectiveness
- •Inclusion Criteria for Investigating Physicians
- •General practitioners practicing:
- •In individual offices, in non-multidisciplinary group practices
- •Or in multidisciplinary health centers or health centers
- •In Nice, Bordeaux, and Lille
- •Who have expressed their non-opposition
- •Willing to participate in the qualitative evaluation
- •Inclusion Criteria for Patients
- •Adult French-speaking patients, able to read and write
- •Suffering from essential uncontrolled and treated hypertension treated measured by home self-monitoring
- •Owning a mobile phone (to be contacted for the study and to receive reminder by phone)
- •Able to self-measure his/her blood pressure at home
- •Who have expressed their non-opposition
- •Inclusion for qualitative interviews Only individuals from the intervention group will be asked to participate in these interviews.
- •All physicians who recruited patients for the trial will be invited to participate.
- •A subsample of 30 patients (10 per city), selected according to the principle of maximum variation (ensuring diversity in age and gender)
排除标准
- •Phase 1: Co-construction of the intervention
- •No exclusion criteria will be applied for this phase.
- •Phase 2: Evaluation of the effectiveness of the intervention
- •Exclusion Criteria for Investigating Physicians
- •GP who participated in the first phase of co-construction.
- •GP from a health center where a collaborator has already been recruited for the study.
- •GP working in collaboration with an Asalée nurse.
- •Exclusion Criteria for Patients
- •Patient suffering from secondary hypertension.
- •Patient with severe cognitive impairment or dementia.
- •Patients already performing regular self-monitoring of their blood pressure.
- •Healthcare professionals.
- •Patient under legal protection, guardianship, or curatorship.
结局指标
主要结局
Proportion of patients with a home-measured blood pressure within the therapeutic target
时间窗: three months after the implementation of the intervention
Proportion of patients with a home-measured blood pressure within the therapeutic target three months after the implementation of the intervention (systolic blood pressure below 140 mm Hg for patients under 80 years old or below 150 mm Hg for patients 80 years and older).
Proportion of patients with a home-measured blood pressure within the therapeutic target
时间窗: three months after the implementation of the intervention
Proportion of patients with a home-measured blood pressure within the therapeutic target three months after the implementation of the intervention (systolic blood pressure below 140 mm Hg for patients under 80 years old or below 150 mm Hg for patients 80 years and older).
次要结局
- Improvement in achieving the target blood pressure six months after the start of the intervention(six months after the intervention)
- Improvement in achieving the target blood pressure at three months after the start of the intervention, in GPs(Three months after the intervention)
- Improvement in achieving the target blood pressure at six months after the start of the intervention, in GPs(Six months after the intervention)
- Health Literacy Level(6 months after the intervention)
- Adherence to treatment scale using Girerd questionnaire(Baseline, three and six months)
- Effect of the Intervention by Social Categories(Baseline, three and six months)
- Effective adoption of tools in the intervention group(At the end of the follow-up, for each patient)
- Perceived effectiveness by patients(During the six months after the end of the trial)
- Perceived effectiveness from the perspective of healthcare professionals(During the six months after the end of the trial)
- Choose and adapt tools of intervention to the context of primary care(Before the beginning of the randomized trial)
- Investigate the factors influencing the acceptability and effectiveness of the LS intervention(Before the beginning of the randomized trial)
- Perceived effectiveness from the perspective of healthcare professionals(During the six months after the end of the trial)
- Choose and adapt tools of intervention to the context of primary care(Before the beginning of the randomized trial)
- Improvement in achieving the target blood pressure six months after the start of the intervention(six months after the intervention)
- Improvement in achieving the target blood pressure at three months after the start of the intervention, in GPs(Three months after the intervention)
- Improvement in achieving the target blood pressure at six months after the start of the intervention, in GPs(Six months after the intervention)
- Health Literacy Level(6 months after the intervention)
- Adherence to treatment scale using Girerd questionnaire(Baseline, three and six months)
- Effect of the Intervention by Social Categories(Baseline, three and six months)
- Effective adoption of tools in the intervention group(At the end of the follow-up, for each patient)
- Perceived effectiveness by patients(During the six months after the end of the trial)
- Investigate the factors influencing the acceptability and effectiveness of the LS intervention(Before the beginning of the randomized trial)