Skip to main content
OpenTrials
Completed

NCT Number: NCT03721848

Impact of a Health and Mental Health Promotion Intervention Among Jordanians and Syrians.

Given the heightened risk of NCDs and mental health issues, it is critical for Jordanians and Syrian refugees to have access to prevention based health services. To address this need, the following project seeks to examine the capacity of Primary Care Health Centers to provide preventive services to empower patients to manage NCDs and potential mental health issues for those who are experiencing distress.

The primary research question in this evaluation study is:

Does prevention-based health and mental health services in primary health clinics improve health status of Jordanians and Syrian refugees?

This research proposal will consist of three study conditions examining:

* Condition 1: an existing NCD preventive intervention consisting of 24 sessions, which are 45 minutes covering diabetes, hypertension, obesity, reproductive health, cardiovascular diseases, allergies and smoking; * Condition 2: The existing NCD preventive intervention with 4 added mental health awareness sessions covering traumatic stress reactions, individual strategies for coping with stress and traumatic events and collective strategies for coping with stress and trauma; * Condition 3: Treatment as usual

A group randomized study will be conducted in three clinics with patients of the respective clinics. The clinics will be identified prior to the study based on similar demographics, service utilization and staff capacity. Once the three clinics are identified they will be selected to one of the three study conditions. This research will be conducted in collaboration with the University of Illinois (UIUC), AmeriCares, and the Royal Health Awareness Society (RHAS) of Jordan. AmeriCares will work as the operational humanitarian organization collaborating with and providing support to RHAS and UIUC. RHAS's healthy community clinic is a community-based health project launched in 2011 conducted with the Ministry of Health (MOH). The project aims to build the capacity of participating Health Centers to provide better preventative services to empower patients to manage their diseases and reduce future complications. The Healthy Community Clinic, established within existing MOH facilities, provides medical practitioners with the training and resources necessary to implement management and prevention-based care to patients in underserved communities.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Mental Stress Behavior Behavioral Symptoms Cardiovascular Diseases Diabetes Diabetes Mellitus Endocrine System Diseases Glucose Metabolism Disorders Hypertension Metabolic Diseases Nutritional and Metabolic Diseases Stress, Psychological Vascular Diseases

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Royal health Awareness Society

Amman, Jordan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Healthy community clinic NCD+MH

Behavioral

NCD+MH Awareness Intervention Overview:

i. Patients are assigned, at minimum, one health awareness lecture per month with a total of 28 lectures possible ii. Patients attend lectures on specific topics given by MoH staff, mainly nurses.

iii. Topics tackled include: Diabetes, Hypertension, Asthma, Cardiovascular Disease, Reproductive Health, Healthy Nutrition, Smoking, Emotional Wellness, Stress Relief and Positive Coping.

iv. Group nutrition and physical fitness counselling are incorporated into most health awareness lectures

Healthy community clinic NCD

Behavioral

i. Patients are assigned, at minimum, one health awareness lecture per month with a total of 24 lectures possible ii. Patients attend lectures on specific topics given by MoH staff, mainly nurses.

iii. Topics tackled include: Diabetes, Hypertension, Asthma, Cardiovascular Disease, Reproductive Health, Healthy Nutrition, and Smoking iv. Group nutrition and physical fitness counselling are incorporated into most health awareness lectures

Primary outcomes

  1. Health Behavior-Fruit Intake frequency (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Likert 5 point question assessing frequency of fruit intake within a week (a. none, b. 1-2 times per week, c. 3-4 times per week, d. 5 + times per week.

  2. Health Behavior-Vegetable Intake (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Likert 5 point question assessing frequency of vegetable intake within a week (a. none, b. 1-2 times per week, c. 3-4 times per week, d. 5 + times per week.

  3. Health Behavior-Bread Intake (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Likert 5 point question assessing frequency of bread intake within a week (a. none, b. 1-2 times per week, c. 3-4 times per week, d. 5 + times per week.

  4. Incidence of Smoking (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Yes/no question asking participants if they smoke. If they answer yet to smoking they are prompted to ask how many cigarettes per week.

  5. Health Behavior- Level of Physical Activity (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Question inquiring how much physical activity participants get per week. Likert question Ranging from a. 30 minutes b.30 min to 1 hour c. 1-2 hours, d. 2-5 hours, e. more than 5 hours

  6. Health Behavior-Amount of Red Meat Intake (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Likert 5 point question assessing frequency of red meat intake within a week (a. none, b. 1-2 times per week, c. 3-4 times per week, d. 5 + times per week.

Secondary outcomes

  1. Duke Health Profile (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Duke Health Profile: 17-item standardized self-report instrument containing six health measures (physical, mental, social, general, perceived health, and self-esteem), and four dysfunction measures (anxiety, depression, pain, and disability).

  2. Blood Pressure (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Trained nurses will collect Blood Pressure: Patients will be asked to remain seated with their legs uncrossed for at least 5 minutes before blood pressure measurements can be taken. In a seated position, systolic and diastolic blood pressure will be measured in mmHg by sphygmomanometer. This measurement should be repeated three times and the average of the second and third measurements should be calculated for data analysis.

  3. BMI (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Patients should be asked to remove their shoes and any outer garments, while maintaining cultural respect. Calibrated scales will be used to measure body weight to the nearest 0.5 kg. Height will be measured to the nearest 0.1 cm using the height rod attached to the scale.23The BMI will be calculated by dividing the mass in Kg over the square of the height in meters according to the equation below:

    BMI = Mass (kg)/Height (m2)

  4. Laboratory tests: fasting blood glucose (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Appointments for laboratory tests will occur in the mornings to allow for patients to fast overnight (a minimum of 8 hours). MedLabs phlebotomists will collect the samples. The amount of blood to be collected is 3 ml. Each tube is clearly marked with the volume of blood to be collected. Any specimen not meeting the test requirement in terms of volume must be rejected.

  5. Laboratory tests: HbA1c (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Appointments for laboratory tests will occur in the mornings to allow for patients to fast overnight (a minimum of 8 hours). MedLabs phlebotomists will collect the samples. The amount of blood to be collected is 3 ml. Each tube is clearly marked with the volume of blood to be collected. Any specimen not meeting the test requirement in terms of volume must be rejected.

  6. Laboratory tests: total cholesterol (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Appointments for laboratory tests will occur in the mornings to allow for patients to fast overnight (a minimum of 8 hours). The amount of blood to be collected is 3 ml. Each tube is clearly marked with the volume of blood to be collected. Any specimen not meeting the test requirement in terms of volume must be rejected.

  7. Health Behavior (Hypertension, Diabetes, Mental health, Nutrition) Knowledge Survey (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    22 item questionnaire developed to measure knowledge of risk and management of: hypertension, diabetes, mental health, nutrition. Participant can report yes/no/I don't know to each question. The correct items will then be summed to identify the levels of knowledge change across time.

  8. Brief Trauma Questionnaire (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Brief Trauma Questionnaire:

    The BTQ is a 10 item self-report questionnaire derived from the Brief Trauma Interview.

  9. Primary Care PTSD (Assessing Change)

    Time frame: Baseline, Six Months, 12 Months, 18 months

    Six item screen derived from the PTSD Checklist-Civilian Version to help primary care settings screen for persons with possible PTSD symptoms. The five point Likert Scale ranges from not at all to extremely inquiring on prevalence of PTSD symptoms (e.g. had repeated disturbing memories about an event; c) Avoided activities or situations because they reminded you of a stressful experience)

Sponsors and collaborators

Lead sponsor

University of Illinois at Urbana-Champaign

Other

Collaborators

  • Americares
  • Royal Health Awareness Society

Registry information

Official study title

Impact of Health Promotion Interventions on the Management and Secondary Prevention of Non-Communicable Diseases Among Jordanians and Syrians in Jordan.

Important dates

Study start
2017
Primary completion
2017
Study completion
2019
First posted
Oct 26, 2018
Registry last updated
Aug 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.