- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06761508
Comparing of Different Visual Aids Like Video,info-graphics and Pamphlets in Enhancing Community Awareness and Promoting Behavioral Change Towards the Prevention of Hypertension in Basilica of the Most Holy Trinity Onitsha Anambra State,Nigeria
January 5, 2025 updated by: Ottiwu Perpetua Chidiogor, Hiroshima University
Comparison of Different Visual Aids in Enhancing Community Awareness and Promoting Behavioral Change in the Prevention of Hypertension in Anambra State,Nigeria
The goal of this observational study is to assess different level of enhanced awareness and behavioral change of adults over the age of 35 who will be educated using video,infographic and pamphlet for the interval of one month
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
81
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Perpetua C Ottiwu, Masters
- Phone Number: +2340832605330
- Email: m232417@hiroshima-u.ac.jp
Study Contact Backup
- Name: Moriyama Michiko, PHD
- Phone Number: +81-82-257-5365
- Email: morimich@hiroshima-u.ac.jp
Study Locations
-
-
Japan
-
Kasumi 1-2-3 Minami-ku, Japan, Nigeria
- Graduate School of Biomedical and Health Sciences Hiroshima University
-
Contact:
- Moriyama Michiko, PHD
- Phone Number: +81-82-257-5365
- Email: morimich@hiroshima-u.ac.jp
-
Contact:
- Clementina Nwankwo, PHD
-
Contact:
- Blessing Onyeje, PHD
-
Contact:
- Babaita Abdulfatia, Masters
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Adults age over 35 years old
- Who does not know his/her blood pressure status within the last 6 months (The person who does not know he or she has a hypertension or not.)
- Who agree to participate
Exclusion Criteria:
- Who cannot come to the church 4 weeks later after the intervention.
- Known hypertensive patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: intervention group using video
Administration of video to the first intervention group
|
A 3 Arm randomized control trial, using video as the first Arm of intervention to assess the behaviour change of the community in hypertension prevention.
|
|
Other: intervention group using infographics
Administration of infographics to the second arm of the intervention group
|
A 3 Arm randomized control trial,that involves the use of infographics in Arm to assess the behaviour change of the community in hypertension prevention.
|
|
Other: control group using pamphlet
Administration of pamphlet to the control groups
|
A 3 Arm randomized control trial,that contains the use of pamphlet for the 3rd Arm which is the control group to assess the behaviour change of the community in hypertension prevention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavioural change in hypertension prevetion
Time Frame: One month
|
Behaviour changes within 1 month related to education - Asking what kind of behaviour change occurred during 1 month Percentage caculation of participants who had behaviour change Each arm: Number of person who changed their behaviour/total number of participants in the arm |
One month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in the awareness level of participants from baseline after 4 week
Time Frame: 4 weeks
|
- Awareness check: Using the Health belief model-The researchers-developed questionnaire:How much they are motivated (pre and post comparison)
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 5, 2025
Primary Completion (Estimated)
February 5, 2025
Study Completion (Estimated)
April 5, 2025
Study Registration Dates
First Submitted
December 15, 2024
First Submitted That Met QC Criteria
January 5, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 5, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MH/COMM/523/VOL.111
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
To ensure confidentiality
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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