The INITIATE Study: Initiating Nicotine Dependence Treatment for Smokers Admitted to Emergency Departments
Ключови думи
Резюме
Дати
Последна проверка: | 04/30/2020 |
Първо изпратено: | 10/06/2019 |
Очаквано записване подадено: | 11/12/2019 |
Първо публикувано: | 11/13/2019 |
Изпратена последна актуализация: | 05/07/2020 |
Последна актуализация публикувана: | 05/10/2020 |
Действителна начална дата на проучването: | 07/31/2020 |
Приблизителна дата на първично завършване: | 06/30/2021 |
Очаквана дата на завършване на проучването: | 10/31/2022 |
Състояние или заболяване
Интервенция / лечение
Behavioral: Quit Card Intervention (QCI)
Фаза
Групи за ръце
Arm | Интервенция / лечение |
---|---|
Experimental: Quit Card Intervention (QCI) Study intervention group. | Behavioral: Quit Card Intervention (QCI) The intervention is comprised of a behavioural incentive in the form of a gift card as well as tailored smoking cessation counseling. Eligible consenting smokers randomized to the QCI group will receive: a "Quit Card" (a gift card worth $300 that can be used to buy nicotine replacement therapies at any pharmacy); self-help information; and, enrollment in six months of telephone follow-up support tailored by treatment goal with a Nicotine Addiction Treatment Specialist. |
No Intervention: Usual Care (UC) Study control group. |
Критерии за допустимост
Възрасти, отговарящи на условията за проучване | 18 Years Да се 18 Years |
Полове, допустими за проучване | All |
Приема здрави доброволци | Да |
Критерии | Inclusion Criteria: - Current daily smoker (smokes ≥ 5 cigarettes per day); - ≥ 18 years of age (the age of majority in Ontario); - Assigned a CTAS level of 2-5 (emergent to non-urgent); - Able to read and understand English or French; - Resides in Ontario and eligible for Ontario Health Insurance Plan (to permit linkage with administrative data housed at the Institute for Clinical Evaluative Sciences [ICES]); - Available and willing to participate in follow-up assessments over the next 24 months; - Has access to a telephone or computer; - Able to provide informed consent Exclusion Criteria: - Currently participating in this or another smoking cessation study; - Assigned a CTAS level of 1 (resuscitation - the most seriously ill patients with highest likelihood of hospital admission) or in psychiatric emergency unit; - Pregnant, planning to become pregnant over the next 2 years, or breastfeeding; - Has morbid illness which will prevent completion of 26-week follow-up (e.g., receiving palliative care); - In the opinion of the ED physician, manifests acute physical and/or psychiatric illness or has cognitive impairment that would preclude participation in/benefit from the intervention. |
Резултат
Първични изходни мерки
1. Smoking Abstinence [26 weeks (6 months) after study enrollment]
Вторични изходни мерки
1. Prolonged Abstinence [4, 26, 52 and 104 weeks after study enrollment]
2. Point Prevalence Abstinence [4, 52 and 104 weeks after study enrollment]
3. Smoking Reduction [4, 26, 52 and 104 weeks after study enrollment]
4. Number of Quit Attempts [4, 26, 52 and 104 weeks after study enrollment]
5. Cessation Medication and/or E-cigarette Use [4, 26, 52 and 104 weeks after study enrollment]
6. Use of Behavioural Supports [4, 26, 52 and 104 weeks after study enrollment]
7. Health-Related Quality of Life [52 and 104 weeks after study enrollment]
8. Health Services Outcomes - ED visits [4, 26, 52 and 104 weeks after study enrollment]
9. Health Services Outcomes - Hospital Admissions [4, 26, 52 and 104 weeks after study enrollment]
10. Health Services Outcomes - Deaths [4, 26, 52 and 104 weeks after study enrollment]
11. Cost-Effectiveness Ratios [52 and 104 weeks after study enrollment]