Assessment of the Health Literacy Among Arab Women in East Jerusalem

Overview

This is a two-stage study: The objective of the first stage is to explore health literacy (HL) needs and preferences of Arab women through conducting Focus Group Discussions (FGDs). The second stage will employ conducting a HL intervention tailored to the participants' needs and preferences as presented in the FGDs. Objectives include increasing the percentage of women who utilize patient-doctor communication skills and increasing their cardiovascular disease (CVD) knowledge.The intervention consists of four sessions that will be conducted in municipality-sponsored women's groups in Jerusalem and other Arab communities. Questionnaires will be completed before and three months after the intervention. The study answers the following: Can HL workshops improve patient-doctor communication skills and CVD knowledge in Arab women.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Non-Randomized
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Prevention
    • Masking: None (Open Label)
  • Study Primary Completion Date: June 30, 2025

Detailed Description

Arab women in Israel are at high risk of low health literacy due to lower levels of education and low socio-economic status. Health literacy (HL) refers to the skills and competencies enabling people to obtain and interpret health information and apply their knowledge to inform health-related decision-making. It's also defined as "the degree to which individuals have the capacity to obtain, understand, and process basic health information and services needed to make appropriate health decisions". The objective of the first stage of the study is to explore health literacy needs and preferences of Arab women through conducting Focus Group Discussions (FGDs) with women in East Jerusalem. Six different focus groups will be conducted at three of the six municipality community centers in East Jerusalem. Participants will be recruited through identified community centers. Each group will meet once for up to two hours. The study will be explained to them by an investigator who has been trained in the administration of focus groups, and they will be asked to sign a consent form. Discussions will be recorded without the names of the participants (they will be instructed not to use their names once the recording begins). At the end of the meeting, each participant will receive a bag and pamphlets with information regarding women's health. The second stage will employ conducting a HL intervention tailored to the participants' needs and preferences as presented in the FGDs. Objectives include increasing the percentage of women who utilize patient-doctor communication skills and increasing their cardiovascular disease (CVD) knowledge.The intervention consists of four sessions that will be conducted in municipality-sponsored women's groups in Jerusalem and other Arab communities. Questionnaires will be completed before and three months after the intervention. The study answers the following: Can HL workshops improve patient-doctor communication skills and CVD knowledge in Arab women.

Interventions

  • Other: Heath literacy assessment in Arab women in East Jerusalem
    • A 4-sessions intervention to increase the participant’s self-efficacy when interacting with their physician and increase their cardiovascular health knowledge.

Arms, Groups and Cohorts

  • No Intervention: Arab Women health literacy focus groups
    • Arab women in East Jerusalem will be part of focus groups. During the focus groups, a set of pre-prepared questions will be presented to the participants. The focus groups will be recorded and analyzed verbatim.
  • Experimental: Health literacy workshop
    • Women from East-Jerusalem and other Arab communities in Israel will be invited to participate in a 4-sessions workshop designed to improve health literacy, self-efficacy when interacting with their physician and increase their cardiovascular health knowledge.

Clinical Trial Outcome Measures

Primary Measures

  • assessment of health literacy level and elucidate factors that will improve health literacy (barriers, incentives, etc.…) among Arab women in East Jerusalem
    • Time Frame: within 6 months
    • The assessment will be done through conduction of focus groups. Focus groups will be audio- recorded, transcribed and analyzed using Systematic text condensation, a descriptive and explorative analysis strategy. Which consists of four steps: 1) total impression – from chaos to themes; 2) identifying and sorting meanings units – from themes to codes; 3) condensation – from code to meaning; 4) synthesizing – from condensation to descriptions and concepts. It is expected that six focus groups will be sufficient to achieve saturation of themes. If results are not sufficient, investigators will ask to increase the number of focus groups.
  • Change in cardiovascular disease knowledge
    • Time Frame: At baseline and three months after intervention
    • A self report questionnaire based on the American Heart Association’s Cardiovascular, and assess the knowledge regarding heart attack symptoms, by answering yes/no to each item.
  • Change in perceived efficacy in patient-physician interaction
    • Time Frame: At baseline and three months after intervention
    • Will be assessed using the 10-item Perceived Efficacy in Patient-Physician Interaction (PEPPI) (Maly, Frank, Marshall, Diametteo, Reuben, 1998). Participants respond to each question on a scale of 1 to 10, with 10 representing “very confident,” and 1 representing “not at all confident”. Higher scores represent positive outcome.
  • Change in remembering doctor’s recommendations and reading blood test results
    • Time Frame: At baseline and three months after intervention
    • A 2-item version derived from the Perceived Efficacy in Patient-Physician Interaction (PEPPI). Participants respond to each question on a scale of 1 to 5, with 5 representing “very confident,” and 1 representing “not at all confident”. Higher scores represent positive outcome.
  • change in health literacy
    • Time Frame: At baseline and three months after intervention
    • Will be assessed using the Health Literacy Survey-Europe-Q16 (HLS-EU-Q16) a 16 question research instrument adapted for use in Israel. Participants respond to each question on a scale of 1 to 4, with 4 representing “fairly easy,” and 1 representing “very difficult”. Higher scores represent positive outcome.
  • Change in preparation for doctor’s visit
    • Time Frame: At baseline and three months after intervention
    • A 6-item questionnaire represents preferred actions that participant\pants do before their doctor appointment. The more items are selected, the higher the score is, hence representing a positive outcome.

Secondary Measures

  • Change in Self-Rated Status of Health (SRH)
    • Time Frame: At baseline and three months after intervention
    • A validated single item health measure in which participants rate the current status of their own health on a five-point scale, from excellent to poor
  • Change in perceived efficacy in reading and understanding the instruction for taking medications
    • Time Frame: At baseline and three months after intervention
    • Participants will be asked “how confident do you feel you are able to follow the instructions on the label of a medication bottle?”

Participating in This Clinical Trial

Inclusion Criteria

  • All women aged 18-85 that attend and participate in the community's women's groups – They must speak Arabic Exclusion Criteria:

  • Not in the age range of 18-85. – Do not speak Arabic.

Gender Eligibility: Female

Minimum Age: 18 Years

Maximum Age: 85 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Hadassah Medical Organization
  • Provider of Information About this Clinical Study
    • Principal Investigator: Donna R Zwas, Director of Linda Joy Pollin Cardiovascular Wellness Center for Women – Hadassah Medical Organization
  • Overall Official(s)
    • Donna Zwas, MD MPH, Principal Investigator, Hadassah Medical Organization
  • Overall Contact(s)
    • Donna Zwas, MD,MPH, +97226779451, dannaz@hadassah.org.il

References

Maly RC, Frank JC, Marshall GN, DiMatteo MR, Reuben DB. Perceived efficacy in patient-physician interactions (PEPPI): validation of an instrument in older persons. J Am Geriatr Soc. 1998 Jul;46(7):889-94. doi: 10.1111/j.1532-5415.1998.tb02725.x.

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