To evaluate the impact of three different implementation strategies for implementing IBSM in current clinical practice, we have proposed the following three hypotheses: 1. Hypothesis 1 (Reach): More general practices will participate in IBSM in the…
ID
Bron
Verkorte titel
Aandoening
Asthma
Ondersteuning
the Netherlands Asthma Foundation (NAF 3.4.09.011)
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Patient participation in IBSM;<br>
2. Patients with a clinically relevant improvement in asthma-related quality of life.
Achtergrond van het onderzoek
Background:
Internet-Based Self-Management (IBSM) support cost-effectively improves asthma control, asthma related quality of life, number of symptom-free days and lung function in patients with mild to moderate persistent asthma. The current challenge is to implement IBSM in clinical practice.
Based on previously detected barriers and facilitators for implementation we developed implementation strategies for IBSM that address these barriers and facilitators.
The aim of this project is to investigate the (cost-) effectiveness of these tailored implementation strategies in comparison to a common used implementation strategy, in a three arm randomized trial.
Study design:
A three-arm cluster randomised trial with a cluster pre-randomisation design and 12 months follow-up per practice comparing the following three IBSM implementation strategies:
1. Basic Implementation Strategy (BIS): dissemination of the IBSM programme (‘PatientCoach’);
2. Start-up Support Implementation Strategy (SSIS): BIS + start-up support for professionals (i.e. support in selection of the appropriate population and training of professionals);
3. Practice Coach Implementation Strategy (PCIS): SSIS + additional training and ongoing support for professionals.
Study population:
Patients with mild to moderate persistent asthma from general practices, age 18-50 yr, need for daily treatment with inhaled corticosteroids (more than 3 months usage of inhaled corticosteroids in the previous year), and will be identified via primary care patient registries in the Leiden region. We aim to evaluate 14 practices that participate in IBSM in all three strategies, involving 140 patients per arm to be invited to for evaluation of IBSM.
Primary outcomes are:
1. Patient participation in IBSM;
2. Patietns with a clincially relevant improvement in asthma-related quality of life.
Secondary outcomes are:
Patient level: clinical outcomes (asthma control, lung function, usage of airway treatment and presence of exacerbations); self-management related outcomes (health education impact, medication adherence and illness perceptions);
Professional and organizational level: adherence of professionals to implementation strategies, experience with IBSM and feasibility of IBSM in daily practice. Cost-effectiveness: cost effectiveness and cost-utility.
Doel van het onderzoek
To evaluate the impact of three different implementation strategies for implementing IBSM in current clinical practice, we have proposed the following three hypotheses:
1. Hypothesis 1 (Reach): More general practices will participate in IBSM in the practice coach- and the Start-up Support Implementation Strategy - as compared to the Basic Implementation Strategy;
2. Hypothesis 2 (Participate): The proportion of referred patients who participate in the IBSM programme in the practice coach- and the Start-up Support Implementation Strategy will be greater as compared to the Basic Implementation Strategy;
3. Hypothesis 3 (Outcome): The proportion of patients who participate in the IBSM programme and have an important improvement in asthma-related quality of life will be greater among those in the practice coach- and the Start-up Support Implementation Strategy will be greater compared to the Basic Implementation Strategy;
4. Hypotheses 4 (Cost-effectiveness): The practice coach- and the start-up implementation strategy will be more cost-effective as compared to the Basic Implementation Strategy.
Onderzoeksopzet
Baseline, 3 and 6 months.
Onderzoeksproduct en/of interventie
The intervention to be implemented, is an Internet Based Selfmanagement (IBSM) application named PatientCoach. It consists of both a generic web-based system (with information on asthma, monitoring, feedback, and a pre defined medication plan) and an instruction visit for patients.
Three implementation strategies for implementating IBSM will be compared:
1. Basic Implementation Strategy (BIS): dissemination of the IBSM programme (‘PatientCoach’);
2. Start-up Support Implementation Strategy (SSIS): BIS + start-up support for professionals (i.e. support in selection of the appropriate population and training of professionals);
3. Practice Coach Implementation Strategy (PCIS): SSIS + additional training and ongoing support for professionals.
Follow-up per patient is six months in the SSIS and PCIS strategies. Patients in the BIS strategy will only be approached for an endpoint evaluation at 6 months.
End-points on the practice level (SSIS and PCIS strategies) will be measured at 12 months after the first invitation letter to the general practice to participate in IBSM. Individual patient outcomes will be evaluated in the PCIS and SSIS-strategy at baseline, 3 and 6 months after a patient’s start with PatientCoach. Individual patient outcomes in the BIS-strategy will be evaluated at 6 months (end-point evaluation) after a patient’s start with PatientCoach.
Publiek
P.O. Box 9600
J.L. Gaalen, van
Albinusdreef 2
[default] 2300 RC
The Netherlands
+31 (0)71 5264920
j.l.van_gaalen@lumc.nl
Wetenschappelijk
P.O. Box 9600
J.L. Gaalen, van
Albinusdreef 2
[default] 2300 RC
The Netherlands
+31 (0)71 5264920
j.l.van_gaalen@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
(All of the following criteria)
1. Age 18-50 yr;
2. Doctors diagnosis of asthma;
3. Patients who need inhaled corticosteroids as controller medication (step 2-4 GINA
guideline) and / or montelukast;
4. Inhaled corticosteroids ≥ 3 months in the previous year;
5. Access to the internet;
6. Written informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Inability to understand written and oral Dutch instructions;
2. Active diseases likely to interfere with the purpose of the study, such as a terminal illness or a severe psychiatric disease;
3. Daily or alternate day oral corticosteroid therapy for at least 1 month before entering the study;
4. Patients who are primarily under treatment by a pulmonologist.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL2829 |
NTR-old | NTR2970 |
Ander register | METC LUMC : P11.077 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |