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WithdrawnNCT04149236deCiPHeRGapUpdated Aug 18, 2023

A Qualitative Study of Cultural Perception of Health in Rural Guatemala

An observational study in Qualitative Research and Beliefs, sponsored by University of Colorado, Denver. Withdrawn. Open to participants aged 18 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-18.

Sponsored by University of Colorado, Denver · Observational

Why this study was withdrawn
Was halted during the COVID pandemic; study continuation plans discontinued as some investigators no longer associated with the University of Colorado.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
0
Ages
18 Years to 64 Years
Sex
All
01

Study summary

The Investigators will be giving a survey to \~100 people in a rural community in Guatemala to discover beliefs and perspectives that the Participants have surrounding various aspects of healthcare. The Investigators aim to do this in order to be able to better serve the population in the community by discovering specific information about them from the Participants and how the Participants about different health practices. The Investigators will answer their research questions through the questionnaire that will allow participants to explain their viewpoints about a variety of medical topics.

Read the detailed description

The design of this cross-sectional study is centered around a structured questionnaire of a mixed qualitative and quantitative nature that is composed primarily of yes/no or Likert scale responses. All questions are written with the intent that they may be understood by those participants without any formal education. The investigators will recruit participants that are currently using the services of the Trifinio clinic in rural Guatemala as these are likely to fit inclusion criteria and will be able to benefit from potential future services that will be directed by the findings of this questionnaire. For all participants, Likert scale questions will be used with a series of faces to help indicate meanings for the answers and to decrease possibility of misinterpretation. Participants will be recruited through non-probabilistic sampling and the use of snowball sampling. Screening of these participants for exclusion criteria will be performed before questionnaires are distributed. The questions of the questionnaire are designed to elicit information about certain beliefs or preferences related to healthcare in a structured manner that allows us to compare answers and determine trends, prevalence, and associations that are likely to exist among community members. Participation will be completely voluntary and informed consent will be obtained from each participant before they are given the questionnaire. For participants who are illiterate or would prefer to have the informed consent and questionnaire read aloud to them, this will be done by one of the CITI-trained investigators. Recorded data will only include questionnaire responses and will not include any identifying information. We will be using randomized numbers in order to refer to completed questionnaires, but these numbers will have no identifying aspects and will be used for the sole purpose of keeping track of the gathered data. The information gathered will be de-identified and stored and password-protected through REDCap.

02

Conditions studied

  • Qualitative Research
  • Beliefs

Keywords

  • Culture
03

In context

Lead sponsor

University of Colorado, Denver is the lead sponsor of 1,499 studies on the registry; 315 are open to participants now.

Of its 139 completed or terminated interventional studies of FDA-regulated products, 89 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

The study population will consist of local rural Guatemalans that live within 50 km of the clinic site that wish to participate in completing a questionnaire to better inform the clinic of community needs, educational opportunities, and available resources.

Inclusion criteria

  • Age 18-64
  • Willing and able to participate in the questionnaire (if participant is illiterate, they will have the option to have each question and all responses read to them aloud by one of the trained researchers)
  • Live in one of the communities within 50 km of the research site
  • Those participants born in Guatemala

Exclusion criteria

Exclusion Criteria:

  • \< 18 or >64 years old
  • Decisionally challenged
  • Refusal or inability to give consent
  • Those born outside of Guatemala
  • Those living in areas > 50 km from the research site
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
0 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Prevalence of Gaps in Knowledge Surrounding Health Services

    A survey with yes/no questions whether a participant is aware of health services available to them. Answers will be scored as 1 = Yes/Aware or 0=No/Not Aware.

    Time frame: Day 1

  2. Perceptions of Healthcare, as Determined by Agreeability of Statements

    Likert scale responses will be shown to participants who will choose among 5 answers ranging from "Very Much So Disagree" to "Very Much So Agree". The answers chosen will be summed and put into percentages that each answer receives, demonstrating prevalence of those beliefs among the participants.

    Time frame: Day 1

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — The Investigators will de-identify participants and pool total data after questionnaire completion. The results of pooled data may be shared but individual participant data will not be.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04149236
Lead sponsor
University of Colorado, Denver
Responsible party
Sponsor
First posted
Nov 4, 2019
Start date
Aug 1, 2019
Primary completion
Aug 11, 2023
Completion
Aug 11, 2023
Last update
Aug 18, 2023

Study contacts

James L Martin
principal investigator · University of Colorado, Denver

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

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