Storytelling Intervention for African Americans Living With Hypertension

NCT ID: NCT05594264

Last Updated: 2024-10-08

Study Results

Results available

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Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-14

Study Completion Date

2023-06-24

Brief Summary

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Narrative communication (e.g., storytelling) is an approach that has contributed to behavioral change for individuals with conditions such as diabetes, breast cancer, and hypertension. The objective of this study is to conduct a feasibility and pilot study storytelling intervention for African Americans with hypertension. In the feasibility phase 30 African Americans with hypertension will be recruited to view nine patient stories and provide feedback on the effectiveness, usefulness, and satisfaction with the stories. Nine African Americans adults with hypertension were filmed, sharing experiences living with and managing hypertension; including, diet and exercise tips, suggestions for locating healthy foods, and motivational stories about successfully controlling hypertension. During the feasibility phase feedback will also be elicited from the participants about the best approaches for delivering a storytelling intervention, and obtain feedback on the resources and health information that would be helpful to an individual participating in a storytelling intervention. In the pilot study phase, 30 African Americans adults with hypertension will be recruited to participate in a 6-week trial, each week the participants will watch one story and review one module of health information accessible through the study specific website developed for the High Blood Pressure Stories (HBPStories) study. Data will be collected at baseline and 6-weeks including systolic and diastolic blood pressure, medication adherence, health behaviors such as diet and physical activity, and psychosocial measures including positive affect and self-efficacy in the management of hypertension.

Detailed Description

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Conditions

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Hypertension

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

The two phase study, included a feasibility phase. During the feasibility phase 30 participants would be recruited to provide feedback on the design of the website, the impact of the study, and preferences for future study designs. The second phase of the study was the pilot study. The objective of the 6-week study was to explore the impact of a web-based storytelling program on medication adherence and blood pressure.
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Pilot Study

The objective of the second phase of the study was to conduct a 6-week pilot study of the web-based storytelling approach

Group Type EXPERIMENTAL

HBPStories

Intervention Type BEHAVIORAL

The objective of this arm was to pilot test the web-based storytelling program to determine the preliminary impact on blood pressure and medication adherence, and if the web-based approach was an engaging approach for individuals managing hypertension.

Feasibility Phase

The objective of the feasibility phase was to assess participant views of the stories and the study website, and obtain feedback for the design of a future trial.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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HBPStories

The objective of this arm was to pilot test the web-based storytelling program to determine the preliminary impact on blood pressure and medication adherence, and if the web-based approach was an engaging approach for individuals managing hypertension.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* self-reported hypertension
* race/ethnicity: Black or African American
* prescribed antihypertensive medication
* age ≥ 18 years

Exclusion Criteria

* cognitive limitations that limit the ability to provide informed consent
* unable to speak or read English
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute of General Medical Sciences (NIGMS)

NIH

Sponsor Role collaborator

University of Delaware

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of Delaware

Newark, Delaware, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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2P20GM113125-06

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1766419-7

Identifier Type: -

Identifier Source: org_study_id

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