IHEAL Trial: Effectiveness of a Health Promotion Intervention for Women Who Have Experienced Intimate Partner Violence

Western University, Canada

Status

Completed

Conditions

Intimate Partner Violence

Treatments

Behavioral: Information about Community Services

Behavioral: iHEAL

Study type

Interventional

Funder types

Other

Identifiers

NCT03573778

111191

Details and patient eligibility

About

Living with an abusive partner has many negative impacts on women's health, safety and the quality of their lives. These issues often continue when women separate, or take steps to separate, from an abusive partner, and can make it more difficult to create a new life. However, few supports are available to help women manage their health and other challenges around the time of separation.

The Intervention for Health Enhancement and Living (iHEAL) was specifically developed to support women at this time. In iHEAL, women work with a Registered Nurse on issues that affect that their health and well-being in 10 and 18 visits that take place in a safe, private location over a 6 month period. The woman decides which issues she would like to work on, with nurses providing personalized help and support that fits with the woman's needs, goals and wishes. This includes helping her connect to local services if she chooses.

The purpose of this study is to learn whether iHEAL can improve the health and quality of life of women who have separated, or are taking steps to separate, from an abusive partner. To do this, 280 Canadian women from 3 provinces will be offered either iHEAL nurse visits or information about community services that they can use on their own. All participants will complete online surveys when they first start the study and 6 12, and 18 months later to examine whether there are changes in their health, quality of life, confidence and/or control. We also want to learn whether iHEAL is more helpful for some groups of women and whether any benefits to women that are identified outweigh the costs of providing the intervention. A small group of ~30-40 women will be asked to take part in an interview about what is was like to take part in this study when they complete the trial so that we can learn how to further improve iHEAL.

Full description

For a detailed description of the study rationale, hypotheses, research questions and methods, please see:

Ford-Gilboe, M., Varcoe, C., Scott-Storey, K. et al. Longitudinal effectiveness of a woman-led, nurse delivered health promotion intervention for women who have experienced intimate partner violence: iHEAL randomized controlled trial. BMC Public Health 24, 398 (2024). https://doi.org/10.1186/s12889-023-17578-4.

Enrollment

331 patients

Sex

Female

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Woman
19 years of age or older
Able to speak, read and understand English
Residing in specific communities in Ontario, British Columbia or New Brunswick
Planning to remain in area for next 6 months
Experienced physical, sexual, and/or psychological abuse, including coercive control from a current or former partner in the previous 12 months
Planning to separate OR in the process of separating OR separated from an abusive partner in the previous 3 years
Has access to the internet, and a safe computer, tablet, or smart phone
Has a safe email address

Exclusion criteria

Man
Under 19 years of age
Cannot read, speak, understand English
Living outside of the selected study sites, or living in the area but planning to relocate within 6 months
No experience of physical, sexual, or psychological abuse, including coercive control, from a current or former partner in the previous 12 months
Planning to stay with an abusive partner OR separated more than 3 years ago
No access to the internet, or safe computer, tablet or smart phone
No access to safe email and mailing address