Personalized self management support for chronically ill patients using the screeningtool SeMaS.

Implementation of personalized self management support using the Self Management Screening questionnaire SeMaS: A study protocol for a cluster randomized trial.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON26503

Enrollment

700

Registered

2013-04-18

Start date

2013-02-01

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients suffering from chronic conditions, including astma, COPD, diabetes mellitus, and people with (an increased risk of) cardiovascular diseases (CVR).

Interventions

The intervention will be delivered on cluster level in the primary care practice. The intervention consists of personalizing self management support using the results of the SeMaS questionnaire. The r

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: 18 or older; 2. Sex: male or female; 3. Having at least one chronic condition, including astma, COPD, diabetes mellitus, increased cardiovascular risk; 4. Having a check up appointment with the practice nurse in the primary practice in the inclusion period.

Exclusion criteria

Exclusion criteria: 1. Age: below 18 years old; 2. Not able to communicate in Dutch.

Design outcomes

Primary

Measure	Time frame
The difference in the level of patient activation after six months compared between the intervention and control arm, measured with the PAM-13 questionnaire.	—

Secondary

Measure	Time frame
The difference in these variables when comparing intervention to the control arm: 1. Number of completed individual care plans at t=6m; 2. The number of referrals to self management interventions (group courses and internet coaches) in the study period; 3. Adherence to these interventions in the study period; 4. The number of referrals to informative websites in the study period; 5. The number of consultations in the general practice and emergency care in the study period; 6. Rapid assessment of physical activity (RAPA) at t=0 and t=6m; 7. Rapid eating assessment for participants – short version (REAP-S) at t=0 and t=6m; 8. 10-item behavior change consortium questionnaire (smoking) at t=0 and t=6m; 9. S-TOFHLA (health literacy) at t=0 and t=6m; 10. Number and type of psychosocial factors from the SeMaS that is discussed with the patient at the planned check-up appointment at t=0.	—

Measure

Time frame

The difference in these variables when comparing intervention to the control arm: 1. Number of completed individual care plans at t=6m; 2. The number of referrals to self management interventions (group courses and internet coaches) in the study period; 3. Adherence to these interventions in the study period; 4. The number of referrals to informative websites in the study period; 5. The number of consultations in the general practice and emergency care in the study period; 6. Rapid assessment of physical activity (RAPA) at t=0 and t=6m; 7. Rapid eating assessment for participants – short version (REAP-S) at t=0 and t=6m; 8. 10-item behavior change consortium questionnaire (smoking) at t=0 and t=6m; 9. S-TOFHLA (health literacy) at t=0 and t=6m; 10. Number and type of psychosocial factors from the SeMaS that is discussed with the patient at the planned check-up appointment at t=0.

—

Contacts

Public ContactN. Eikelenboom

UMC St Radboud PO Box 9101

n.eikelenboom@iq.umcn.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)