Improving Lifejacket Wear Among Boaters on Lake Albert, Uganda
Primary Purpose
Drowning
Status
Recruiting
Phase
Not Applicable
Locations
Uganda
Study Type
Interventional
Intervention
Peer-led training on lifejacket wear
Sponsored by
About this trial
This is an interventional prevention trial for Drowning focused on measuring Drowning prevention, Occupational boating, Uganda
Eligibility Criteria
Inclusion Criteria:
- The landing sites (clusters) should not be flooded, should not be receiving any known educational/behavior related intervention except the routine marine police messages
Exclusion Criteria:
- Landing sites that are inaccessible because of the bad terrain and poor security
Sites / Locations
- Makerere University School of Public HealthRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Intervention
Control
Arm Description
The peers will be trained to train their colleagues (fellow boaters) on proper lifejacket use. A training manual has been developed for this.
The Marine Police will be encouraged to continue conducting their community policing on water safety and emphasize lifejacket wear.
Outcomes
Primary Outcome Measures
Change in prevalence of lifejacket wear among the boaters
The intention to treat analysis will be used to assess the change in prevalence of lifejacket wear among the boaters. Multilevel modeling (cluster level model and boater level model) with a focus on the individual as the unit of analysis while accounting for clustering will be conducted. The generalized estimating equation (GEE) will be used to account for within-cluster variations. The goodness of fit of the model will be tested using the Hosmer Lemeshow test. Comparison between the baseline and end-line will be done and the difference in differences (Diff in Diff) will be reported to show the change of effect in the intervention and control arm.
Secondary Outcome Measures
Full Information
NCT ID
NCT05337761
First Posted
April 4, 2022
Last Updated
May 16, 2022
Sponsor
Makerere University
Collaborators
Consortium for Advanced Research Training in Africa (CARTA)
1. Study Identification
Unique Protocol Identification Number
NCT05337761
Brief Title
Improving Lifejacket Wear Among Boaters on Lake Albert, Uganda
Official Title
Improving Lifejacket Wear Among Boaters on Lake Albert, Uganda. A Cluster-randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 25, 2022 (Actual)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
October 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Makerere University
Collaborators
Consortium for Advanced Research Training in Africa (CARTA)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A cluster randomized trial will be conducted for six months. To avoid covariate imbalance at baseline, stratified permuted block randomization with a 1:1 allocation ratio will be done. At least 387 boaters across 7 clusters per arm will be interviewed post baseline to give a 90% power to detect the effect of the intervention if such effect exists. A mixed effects multi-level modeling at 5% alpha level will be done using logical model building procedures
Detailed Description
Given that the intervention will be at the community level, a cluster randomized controlled trial is considered most appropriate for testing the hypothesis of this study. The intact groups/clusters of individuals (boaters) rather than individuals themselves, will be randomized to either intervention or control arm. The landing sites herein referred to as clusters, will be the randomization unit. This is because it is difficult to randomize individuals to behavioral intervention since they mix within the cluster. This study will be conducted using an etic epistemological approach guided by a realist ontology in order to objectively measure the effect of the intervention without the influence of the researchers.
To reduce covariate imbalance and increase comparability at baseline, clusters will be randomized to either intervention or control arm using stratified permuted block randomization, with landing sites (clusters) as the randomization unit. The clusters will be stratified by estimated population size and baseline prevalence of lifejacket use as compared with the overall average prevalence. All individuals in the intervention cluster will receive the intervention. The main aim of the stratified randomization is to ensure that the clusters are as comparable as possible at baseline. The other factors that might be considered for stratification will be identified at baseline and, in the opinion of the investigator, might interfere with the objectives of the study. Because there are few clusters per arm (7), two strata will be formed. The stratification variable will be the baseline prevalence of lifejacket wear in the landing sites.
The risk of contamination (one of the major threats to this study) will be reduced by ensuring that at least one cluster which is not part of the study acts as a buffer. From each stratum, one cluster will be randomly allocated to the intervention arm and the other to the control arm using stratified permuted block randomization with a 1:1 allocation ratio. The allocation will be generated using the 'sealed envelope TM' web-based application by an independent statistician who has no interest in the study. The block sizes will be masked/blinded to increase the randomness.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Drowning
Keywords
Drowning prevention, Occupational boating, Uganda
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster randomized trial
Masking
Participant
Masking Description
The study participants will not know if they are receiving the intended intervention or not, since the control arm will also be receiving some messages
Allocation
Randomized
Enrollment
387 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
The peers will be trained to train their colleagues (fellow boaters) on proper lifejacket use. A training manual has been developed for this.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
The Marine Police will be encouraged to continue conducting their community policing on water safety and emphasize lifejacket wear.
Intervention Type
Behavioral
Intervention Name(s)
Peer-led training on lifejacket wear
Intervention Description
Training on proper lifejacket wear will be given to peers who will be the change agents amongst their fellow boaters
Primary Outcome Measure Information:
Title
Change in prevalence of lifejacket wear among the boaters
Description
The intention to treat analysis will be used to assess the change in prevalence of lifejacket wear among the boaters. Multilevel modeling (cluster level model and boater level model) with a focus on the individual as the unit of analysis while accounting for clustering will be conducted. The generalized estimating equation (GEE) will be used to account for within-cluster variations. The goodness of fit of the model will be tested using the Hosmer Lemeshow test. Comparison between the baseline and end-line will be done and the difference in differences (Diff in Diff) will be reported to show the change of effect in the intervention and control arm.
Time Frame
Six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
The landing sites (clusters) should not be flooded, should not be receiving any known educational/behavior related intervention except the routine marine police messages
Exclusion Criteria:
Landing sites that are inaccessible because of the bad terrain and poor security
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Frederick Oporia, MPH
Phone
+256703857428
Email
foporia@musph.ac.ug
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frederick Oporia, MPH
Organizational Affiliation
Makerere University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Makerere University School of Public Health
City
Kampala
ZIP/Postal Code
P.O.Box:7072
Country
Uganda
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Frederick Oporia
Phone
0703857428
Email
foporia@musph.ac.ug
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be shared with the PhD supervisory team
IPD Sharing Time Frame
Six months from the start of the study, and will be accessible to the team until completion of PhD graduation
IPD Sharing Access Criteria
Data will be accessed using password protected external drives
Citations:
PubMed Identifier
1949887
Citation
Bennett S, Woods T, Liyanage WM, Smith DL. A simplified general method for cluster-sample surveys of health in developing countries. World Health Stat Q. 1991;44(3):98-106.
Results Reference
result
PubMed Identifier
21513547
Citation
Michie S, van Stralen MM, West R. The behaviour change wheel: a new method for characterising and designing behaviour change interventions. Implement Sci. 2011 Apr 23;6:42. doi: 10.1186/1748-5908-6-42.
Results Reference
result
Learn more about this trial
Improving Lifejacket Wear Among Boaters on Lake Albert, Uganda
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