My Health eSnapshot - A Preconception Health Research Study

NCT ID: NCT02746601

Last Updated: 2020-05-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-29

Study Completion Date

2017-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of the research is to identify the prevalence of preconception health (PCH) risk factors in the Wellington-Dufferin-Guelph (WDG) catchment area and to determine whether or not a client-driven electronic preconception health risk assessment tool "My Health eSnapshot", for use during healthcare visits, will increase preconception health knowledge and behaviour change among women of reproductive age (15-49 years).

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The purpose of the project is:

1. To develop a client-driven electronic preconception health client risk assessment tool for use in a primary care setting.
2. To develop a customized key message handout for patients based on their risk assessment results.
3. To determine a successful and sustainable process for healthcare providers (HCPs) to administer the risk assessment tool and discuss results with patients within their primary care setting.
4. To increase participants' knowledge of preconception health and their risk factors as a results of the risk assessment tool and discussion with their HCP.
5. To modify participants' health behaviours as a result of the risk assessment tool and discussion with their HCP.
6. To increase WDG Public Health's understanding of the most prevalent preconception health risk factors among reproductive women in WDG.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Preconception Care Health Information Technology Primary Health Care Risk Assessment

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Risk Assessment, Counselling & Resources

Patients complete an electronic preconception health risk assessment tool. Results from the tool are directly uploaded or scanned into the patients' electronic medical record. A healthcare provider provides behavioural counselling, based on results of the risk assessment. Patients are given a customized handout that includes health recommendations and resources based on the patient's identified risk factors.

Group Type EXPERIMENTAL

Risk Assessment, Counselling & Resources

Intervention Type BEHAVIORAL

A risk assessment tool is completed on a tablet. The results are scanned into the patient's electronic medical record. A healthcare provider gives behavioural counselling on identified risk factors. The patient is given a customized handout that includes health recommendations and resources based on the participant's identified risk factors.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Risk Assessment, Counselling & Resources

A risk assessment tool is completed on a tablet. The results are scanned into the patient's electronic medical record. A healthcare provider gives behavioural counselling on identified risk factors. The patient is given a customized handout that includes health recommendations and resources based on the participant's identified risk factors.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Women of reproductive age (15-49 years)
* Not pregnant and have not had a hysterectomy
* A resident of the Wellington-Dufferin-Guelph catchment area
* Able to read and write in English
* Have a valid email address
* Willing to create a unique identifier code during the study to protect their identify
* Are comfortable using a tablet

Exclusion Criteria

\-
Minimum Eligible Age

15 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Guelph

OTHER

Sponsor Role collaborator

Boston Medical Center

OTHER

Sponsor Role collaborator

East Wellington Family Health Team

UNKNOWN

Sponsor Role collaborator

Minto-Mapleton Family Health Team

UNKNOWN

Sponsor Role collaborator

Upper Grand Family Health Team

UNKNOWN

Sponsor Role collaborator

Norfolk Family Medical

UNKNOWN

Sponsor Role collaborator

Wellington-Dufferin-Guelph Public Health

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Minto-Mapleton Family Health Team

Drayton, Ontario, Canada

Site Status

East Wellington Family Health Team

Erin, Ontario, Canada

Site Status

Upper Grand Family Health Team

Fergus, Ontario, Canada

Site Status

Norfolk Family Medical

Guelph, Ontario, Canada

Site Status

University of Guelph

Guelph, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2016-1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The Ebeltoft Health Promotion Project
NCT00145782 COMPLETED PHASE3
The Healing Circles Project
NCT03159325 COMPLETED NA
Healthy Lifetime - Phase 2
NCT05920733 RECRUITING NA
iControl Chronic Kidney Disease
NCT03951363 TERMINATED NA