Impact of a Health and Mental Health Promotion Intervention Among Jordanians and Syrians.
Mental Stress, Hypertension, Diabetes
About this trial
This is an interventional prevention trial for Mental Stress
Eligibility Criteria
Inclusion Criteria:Eligible patients are referred to the study through the treating MOH physicians at the health centers. Through an initial screening process, patients will be assessed for eligibility via inclusion/exclusion criteria by trained nurses. As stated, the nurses will be trained in the data collection procedures by the Research Manager and potential subjects will be fully informed that they can still receive health care services even if they have no interest in participating in the research. This information will be received through the patient information and self-report.
Inclusion Criteria (at least two of the following):
- Obesity, defined as BMI ≥ 30
- Fasting blood glucose ≥ 100 ml/dl
- Systolic blood pressure ≥ 120 mmHg and/or diastolic blood pressure ≥ 80 mmHg
- Self-reported uncontrolled dyslipidaemia, cholesterol >240, LDL >190, HDL < 40 ad/or TG >500
- Asthma
- Diabetes
- Hypertension
Exclusion Criteria:
Exclusion criteria:
- Renal dysfunction: also known as renal insufficiency or renal failure; assessed by self-report
- Heart failure: also known as congestive heart disease or chronic heart failure; assessed by self-report
- Functional disability: defined as any long-term activity limitation due to disease or injury; assessed by self-report
- Liver dysfunction: also known as liver failure, acute or chronic; assessed by self-report
- Uncontrolled Resistant Hypertension: defined as blood pressure remaining above the threshold despite lifestyle modifications and concurrent use of at least three antihypertensive medications from different classes with one being a diuretic10-11assessed by self-report
- Pregnant women
- Uncontrolled Hypothyroidism * Pregnant women are excluded because it would be almost impossible to find any reduction in pregnant women weight and that will show a negative impact of HCC intervention on weight reduction. Therefore, inclusion of pregnant women could be a confounding factor to the study.
Sites / Locations
- Royal health Awareness Society
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Healthy Community Clinic: NCD+MH
Healthy Community Clinic: NCD
Treatment as usual
The arm of this study consists of a 28 session intervention, which are 45 minutes and meet 2-3 times a month providing health awareness on non-communicable diseases diabetes, hypertension, obesity, reproductive health, cardiovascular diseases, allergies; smoking; traumatic stress reactions, individual strategies for coping with stress and traumatic events and collective strategies for coping with stress and trauma.
The arm of this study consists of a 24 session intervention, which are 45 minutes and meet 2 times a month providing health awareness on non-communicable disease diabetes, hypertension, obesity, reproductive health, cardiovascular diseases, allergies; smoking.
This is treatment as usual where there is no intervention, but patients attend the clinic for treatment of non-communicable diseases.