Social Media Use in Sickle Cell Patients

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05182216

Enrollment

Registered

2022-01-10

Start date

2023-01-01

Completion date

2023-12-31

Last updated

2023-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Survey, Family Life

Brief summary

Surveys of patients to identify primary social media sources for health news.

Interventions

None listed

Study design

Observational model

ECOLOGIC_OR_COMMUNITY

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* sickle cell disease diagnosis

Exclusion criteria

* negative sickle cell disease diagnosis

Design outcomes

Primary

Measure	Time frame	Description
Social Media Use in Sickle Cell Patients	six months	Surveys. The survey will have a variety of social media options and ask participants to select the medium used to receive information on health, news, and entertainment.

Outcome results