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OpenTrials
Completed

NCT Number: NCT02309528

Chronic Kidney Disease Knowledge and Awareness Among American Indians

Few educational intervention clinical trials have been conducted among those at risk for or with early chronic kidney disease. To the investigators' knowledge none have used digital storytelling as a means to deliver the educational message and have been conducted among American Indians, a group with high prevalence of chronic kidney disease and end stage kidney disease.

The aims of the research project are to:

1. Quantify levels of chronic kidney disease knowledge and awareness among American Indians. 2. Determine the effectiveness of a culturally tailored health presentation with computerized digital stories made by American Indians for improving chronic kidney disease knowledge and factors thought to be preventative of chronic kidney disease or its progression at baseline and follow-up in a pilot educational clinical intervention trial.

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Key information

Conditions

Chronic Kidney Disease Chronic Disease Disease Attributes Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Kidney Diseases Male Urogenital Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms Renal Insufficiency Renal Insufficiency, Chronic Urogenital Diseases Urologic Diseases

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Strong Heart Study or Strong Heart Family Study participant

Exclusion criteria

  • End Stage Renal Disease

Treatment and study plan

Educational computerized digital stories

Other

computerized digital stories made by American Indians

Primary outcomes

  1. Chronic Kidney Disease Knowledge

    Time frame: up to 12 months

    Survey of CKD Knowledge at baseline, post-intervention, 1-month follow up, 6 month follow up, and 12 month follow up

Secondary outcomes

  1. Blood Pressure

    Time frame: Sept 2014-Sept 2015, baseline, 1-month, 6-month, and 12-month follow-up

    average resting blood pressure collected via automated BP machine which has 5 minute rest period, then collects BP at 1 minute intervals for 3 measurements, and then calculates an average

  2. Self-reported doctor visits and hospitalizations

    Time frame: 1-month, 6-month, and 12-month follow-up

    Survey collection of self-reported doctor visits or hospitalizations

  3. Self-reported new medical conditions

    Time frame: 1-month, 6-month, and 12-month follow-up

    Survey collection of self-reported new diagnoses (i.e. diabetes, hypertension)

  4. Self-reported medication use and adherence

    Time frame: 1-month, 6-month, and 12-month follow-up

    Self-reported non-steroidal anti-inflammatory use and self-reported medication adherence of diabetes and/or blood pressure medications via the Morisky Medication Adherence Scale (MMAS-4)

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Dec 5, 2014
Registry last updated
Aug 30, 2016

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.

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