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#SafeHandsSafeHearts: An eHealth Intervention for COVID-19 Prevention and Support (COVID-19)

Primary Purpose

Covid19

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
eHealth for Covid-19 prevention and support
Sponsored by
University of Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Covid19 focused on measuring COVID-19, Protective behaviors, LGBT populations, Racialized populations, Social determinants of health, Randomized controlled trial, Psychoeducation, Motivational-interviewing, Low- and middle-income countries, Psychological distress

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years or older
  • Self-identified as LGBT+
  • Lived in the study locale (city/region) for at least 6 months
  • Plan to remain in the study locale (city/region) for at least 3 months

Exclusion Criteria:

  • Located outside of Greater Toronto and Hamilton Area (Canada), Mumbai/Thane (India) or Bangkok metropolitan area (Thailand)

Sites / Locations

  • Women's Health in Women's HandsRecruiting
  • Humsafar Trust
  • Institute of HIV Research and Innovation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Immediate

Waitlist

Arm Description

Behavioral: Motivational interviewing (MI)-based peer counseling: MI-based peer counseling will comprise of 3 weekly 1-hour sessions administered online addressing 1) Covid-19 knowledge; 2) Assessing risk for infection and understanding and practicing public health-recommended protective behaviors (masking, physical distancing, handwashing); and 3) Understanding psychosocial issues and maintaining mental wellness.

Behavioral: Motivational interviewing (MI)-based peer counseling: After the immediate group completes the intervention, the waitlist group will receive the intervention. MI-based peer counseling will comprise of 3 weekly 1-hour sessions administered online addressing 1) Covid-19 knowledge; 2) Assessing risk for infection and understanding and practicing public health-recommended protective behaviors (masking, physical distancing, handwashing); and 3) Understanding psychosocial issues and maintaining mental wellness.

Outcomes

Primary Outcome Measures

Change in COVID-19 knowledge
COVID-19 transmission knowledge (index of 8 items, minimum score = 0 - maximum score = 8, higher score = greater knowledge/better outcome, based on CDC, 2020 [June 30])
Change in COVID-19 protective behaviors
Mask wearing, physical distancing, handwashing (index of 9 items, minimum score = 0 - maximum score = 18, higher score = better outcome; based on CDC, 2020 [July 31])
Change in depressive symptoms
Frequency of depressed mood and anhedonia (Patient Health Questionnaire 2 [PHQ-2], minimum score = 0, maximum score = 6; higher score = worse outcome)
Change in anxiety symptoms
Frequency of anxiety symptoms (Generalized Anxiety Disorder 2 [GAD-2], minimum score = 0, maximum score = 6; higher score = worse outcome)

Secondary Outcome Measures

Change in loneliness/social isolation
Frequency of feeling lonely/socially isolated (Three-Item Loneliness Scale, minimum score = 0, maximum score = 6; higher score = worse outcome)

Full Information

First Posted
April 23, 2021
Last Updated
May 23, 2022
Sponsor
University of Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT04870723
Brief Title
#SafeHandsSafeHearts: An eHealth Intervention for COVID-19 Prevention and Support
Acronym
COVID-19
Official Title
An International Multi-site, Randomized Controlled Trial of a Brief eHealth Intervention to Increase COVID-19 Knowledge and Protective Behaviors, and Reduce Pandemic Stress Among Diverse LGBT+ People
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
May 15, 2022 (Actual)
Study Completion Date
July 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Toronto

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
This project seeks to test the efficacy of a brief eHealth intervention in an international randomized controlled trial (RCT) to increase COVID-19 knowledge and protective behaviors, and reduce psychological distress among LGBT people. This project involves enrolling racially diverse samples of lesbian, gay, bisexual and transgender people in three cities, randomizing 900 people (stratified among cisengender men, cisgender women, and transgender people) to either the immediate behavioral intervention or the waitlist control condition. Participants will complete a baseline survey, a follow-up survey 2 weeks post-intervention, and a final survey 2 months after the post-intervention survey. Primary outcomes are COVID-19 transmission knowledge, COVID-19 protective behaviors, and psychological distress.
Detailed Description
Lesbian, gay, bisexual, and transgender (LGBT+) populations are at heightened vulnerability to COVID-19 due to existing health disparities amid adverse social determinants of health (SDOH), rights violations, and social-structural constraints on public health recommended (PHR) protective measures. Yet, public health responses largely do not address LGBT+ vulnerabilities nor do they include LGBT+ communities in pandemic response planning. As there is no manualized intervention for COVID-19 prevention, the investigators will adapt an efficacious eHealth intervention for preventing HIV infection and transmission, the deadliest pandemic of the last century. This study builds on evidence-based eHealth interventions using Motivational Interviewing (MI) and Psychoeducation to increase health knowledge and behaviors, and reduce psychological distress, including interventions with LGBT+ people. MI is a client-centered counseling approach that elicits and strengthens intrinsic motivation for change. Psychoeducation integrates education and counseling to promote mental health. Peer counselors will receive 5 days of online training on COVID-19, PHR behaviors, pandemic stress (anxiety, depression, social isolation), MI-based counselling, psychoeducation, and research ethics. The 3 primary study outcomes are increasing COVID-19 knowledge, PHR protective behaviors, and reducing psychological distress; these are crucial elements of public health approaches to control SARS-CoV-2 transmission. #SafeHandsSafeHearts is a 3-session peer-delivered MI-based brief counselling (45 min-1 hr) with weekly individual sessions. Participants will be recruited online with electronic flyers and social media messages developed with community-based organization (CBO) partners, and distributed through CBO social media accounts and listservs in each of the three study sites (Toronto, Bangkok, Mumbai), and a study website. Participants will be randomized to the immediate intervention group or waitlist control group at a 1:1 ratio, stratified by sex and gender (cisgender men, cisgender women, transgender people), using a computer-generated sequence. All participants will complete a baseline survey, a post-intervention follow-up survey 2 weeks after completing the intervention, and a final survey 2 months after post-intervention survey. NOTE: Due to pandemic-related delays and lockdowns, and Toronto site approvals and opening 6-months prior to Bangkok and Mumbai, Toronto site is a pilot intervention to inform feasibility, acceptability, and implementation of the RCT; Bangkok and Mumbai sites remain RCTs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19
Keywords
COVID-19, Protective behaviors, LGBT populations, Racialized populations, Social determinants of health, Randomized controlled trial, Psychoeducation, Motivational-interviewing, Low- and middle-income countries, Psychological distress

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
900 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Immediate
Arm Type
Experimental
Arm Description
Behavioral: Motivational interviewing (MI)-based peer counseling: MI-based peer counseling will comprise of 3 weekly 1-hour sessions administered online addressing 1) Covid-19 knowledge; 2) Assessing risk for infection and understanding and practicing public health-recommended protective behaviors (masking, physical distancing, handwashing); and 3) Understanding psychosocial issues and maintaining mental wellness.
Arm Title
Waitlist
Arm Type
Other
Arm Description
Behavioral: Motivational interviewing (MI)-based peer counseling: After the immediate group completes the intervention, the waitlist group will receive the intervention. MI-based peer counseling will comprise of 3 weekly 1-hour sessions administered online addressing 1) Covid-19 knowledge; 2) Assessing risk for infection and understanding and practicing public health-recommended protective behaviors (masking, physical distancing, handwashing); and 3) Understanding psychosocial issues and maintaining mental wellness.
Intervention Type
Behavioral
Intervention Name(s)
eHealth for Covid-19 prevention and support
Intervention Description
3-session online peer-counseling intervention based on motivational interviewing and psychoeducation
Primary Outcome Measure Information:
Title
Change in COVID-19 knowledge
Description
COVID-19 transmission knowledge (index of 8 items, minimum score = 0 - maximum score = 8, higher score = greater knowledge/better outcome, based on CDC, 2020 [June 30])
Time Frame
Baseline survey, 2-week post-intervention survey, and 2-month post-intervention survey
Title
Change in COVID-19 protective behaviors
Description
Mask wearing, physical distancing, handwashing (index of 9 items, minimum score = 0 - maximum score = 18, higher score = better outcome; based on CDC, 2020 [July 31])
Time Frame
Baseline survey, 2-week post-intervention survey, and 2-month post-intervention survey
Title
Change in depressive symptoms
Description
Frequency of depressed mood and anhedonia (Patient Health Questionnaire 2 [PHQ-2], minimum score = 0, maximum score = 6; higher score = worse outcome)
Time Frame
Baseline survey, 2-week post-intervention survey, and 2-month post-intervention survey
Title
Change in anxiety symptoms
Description
Frequency of anxiety symptoms (Generalized Anxiety Disorder 2 [GAD-2], minimum score = 0, maximum score = 6; higher score = worse outcome)
Time Frame
Baseline survey, 2-week post-intervention survey, and 2-month post-intervention survey
Secondary Outcome Measure Information:
Title
Change in loneliness/social isolation
Description
Frequency of feeling lonely/socially isolated (Three-Item Loneliness Scale, minimum score = 0, maximum score = 6; higher score = worse outcome)
Time Frame
Baseline survey, 2-week post-intervention survey, and 2-month post-intervention survey

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
Self-identified as LGBT+
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years or older Self-identified as LGBT+ Lived in the study locale (city/region) for at least 6 months Plan to remain in the study locale (city/region) for at least 3 months Exclusion Criteria: Located outside of Greater Toronto and Hamilton Area (Canada), Mumbai/Thane (India) or Bangkok metropolitan area (Thailand)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter A Newman, PhD
Phone
416-946-8611
Email
p.newman@utoronto.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Suchon Tepjan
Phone
416-946-7885
Email
suchon.tepjan@utoronto.ca
Facility Information:
Facility Name
Women's Health in Women's Hands
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B1J3
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Monte-Angel Richardson, MSW
Phone
416-593-7655
Email
shshstudy@whiwh.com
Facility Name
Humsafar Trust
City
Mumbai
State/Province
Maharashtra
ZIP/Postal Code
110065
Country
India
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shruta Rawat, MSc
Phone
+91-22-26673800
Email
shruta@humsafar.org
Facility Name
Institute of HIV Research and Innovation
City
Bangkok
ZIP/Postal Code
10500
Country
Thailand
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sataporn Waewklaihong, M.Ed.
Phone
+66-2-253-0996
Email
sataporn@ihri.org

12. IPD Sharing Statement

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Links:
URL
https://www.cdc.gov/coronavirus/2019-ncov/prevent-getting-sick/prevention.html
Description
CDC, 2020. How to Protect Yourself & Others
URL
https://stacks.cdc.gov/view/cdc/89938
Description
CDC, 2020. Stop the spread of rumors

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#SafeHandsSafeHearts: An eHealth Intervention for COVID-19 Prevention and Support

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