Margot Jager
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Margot Jager has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
Andrea F. De Winter
Department of Health Sciences, University Medical Center Groningen, University of Groningen, Antonius Deusinglaan 1/FA10, 9713 AV, Groningen, The Netherlands
4 shared publications- Erik J. Knorth
University of Groningen
4 shared publications Janneke Metselaar
Department of Special Needs Education and Youth Care, University of Groningen, Groningen, the Netherlands
4 shared publications- Sijmen A. Reijneveld
Department of Health Sciences, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands
4 shared publications - Amanda Whittal
Department of Psychology & Methods, Jacobs University Bremen, Campus Ring 1, 28759 Bremen, Germany
1 shared publication - Andrea F. de Winter
Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
1 shared publication
Latest Publications
- Open Access
- 5 November 2019
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 16 (21) , 4300
Patient Perspectives to Inform a Health Literacy Educational Program: A Systematic Review and Thematic Synthesis of Qualitative Studies
Patient-centred care is tailored to the needs of patients and is necessary for better health outcomes, especially for individuals with limited health literacy (LHL). However, its implementation remains challenging. The key to effectively address patient-centred care is to include perspectives of patients with LHL within the curricula of (future) healthcare providers (HCP). This systematic review aimed to explore and synthesize evidence on the needs, experiences and preferences of patients with LHL and to inform an existing educational framework. We searched three databases: PsychInfo, Medline and Cinahl, and extracted 798 articles. One-hundred and three articles met the inclusion criteria. After data extraction and thematic synthesis, key themes were identified. Patients with LHL and chronic diseases encounter multiple problems in the care process, which are often related to a lack of person-centeredness. Patient perspectives were categorized into four key themes: (1) Support system; (2) Patient self-management; (3) Capacities of HCPs; (4) Barriers in healthcare systems. “Cultural sensitivity” and “eHealth” were identified as recurring themes. A set of learning outcomes for (future) HCPs was developed based on our findings. The perspectives of patients with LHL provided valuable input for a comprehensive and person-centred educational framework that can enhance the relevance and quality of education for (future) HCPs, and contribute to better person-centred care for patients with LHL.
- 5 November 2019
- Published by MDPI AG in International Journal of Environmental Research and Public Health
- Vol. 16 (21) , 4300
Open AccessPatient Perspectives to Inform a Health Literacy Educational Program: A Systematic Review and Thematic Synthesis of Qualitative Studies
Patient-centred care is tailored to the needs of patients and is necessary for better health outcomes, especially for individuals with limited health literacy (LHL). However, its implementation remains challenging. The key to effectively address patient-centred care is to include perspectives of patients with LHL within the curricula of (future) healthcare providers (HCP). This systematic review aimed to explore and synthesize evidence on the needs, experiences and preferences of patients with LHL and to inform an existing educational framework. We searched three databases: PsychInfo, Medline and Cinahl, and extracted 798 articles. One-hundred and three articles met the inclusion criteria. After data extraction and thematic synthesis, key themes were identified. Patients with LHL and chronic diseases encounter multiple problems in the care process, which are often related to a lack of person-centeredness. Patient perspectives were categorized into four key themes: (1) Support system; (2) Patient self-management; (3) Capacities of HCPs; (4) Barriers in healthcare systems. “Cultural sensitivity” and “eHealth” were identified as recurring themes. A set of learning outcomes for (future) HCPs was developed based on our findings. The perspectives of patients with LHL provided valuable input for a comprehensive and person-centred educational framework that can enhance the relevance and quality of education for (future) HCPs, and contribute to better person-centred care for patients with LHL.
- Open Access
- 22 October 2018
- Published by Ubiquity Press, Ltd. in International Journal of Integrated Care
- Vol. 18 (s2)
Improving self-management of health through an eHealth application: an action-based study among older adults living in the community
- 22 October 2018
- Published by Ubiquity Press, Ltd. in International Journal of Integrated Care
- Vol. 18 (s2)
Open AccessImproving self-management of health through an eHealth application: an action-based study among older adults living in the community
- Open Access
- 13 September 2016
- Published by Springer Nature in European Child & Adolescent Psychiatry
- Vol. 26 (4) , 403-412
Less reduction of psychosocial problems among adolescents with unmet communication needs
Patient-professional communication has been suggested to be a major determinant of treatment outcomes in psychosocial care for children and adolescents. However, the mechanisms involved are largely unknown and no longitudinal studies have been performed. Our aim was, therefore, to assess over the course of 1 year, the impact of patient-centered communication on psychosocial problems of adolescents in psychosocial care, including the routes mediating this impact. We obtained data on 315 adolescents, aged 12–18 years, enrolled in child and adolescent social or mental health care. We assessed patient-centered communication by comparing the needs and experiences of adolescents with regard to three aspects of communication: affective quality, information provision, and shared decision-making. Changes in psychosocial problems comprised those reported by adolescents and their parents between baseline and 1 year thereafter. Potential mediators were treatment adherence, improvement of understanding, and improvement in self-confidence. We found a relationship between unmet needs for affective quality, information provision, and shared decision-making and less reduction of psychosocial problems. The association between the unmet need to share in decision-making and less reduction of psychosocial problems were partially mediated by less improvement in self-confidence (30 %). We found no mediators regarding affective quality and information provision. Our findings confirm that patient-centered communication is a major determinant of treatment outcomes in psychosocial care for adolescents. Professionals should be aware that tailoring their communication to individual patients’ needs is vital to the effectiveness of psychosocial care.
- 13 September 2016
- Published by Springer Nature in European Child & Adolescent Psychiatry
- Vol. 26 (4) , 403-412
Open AccessLess reduction of psychosocial problems among adolescents with unmet communication needs
Patient-professional communication has been suggested to be a major determinant of treatment outcomes in psychosocial care for children and adolescents. However, the mechanisms involved are largely unknown and no longitudinal studies have been performed. Our aim was, therefore, to assess over the course of 1 year, the impact of patient-centered communication on psychosocial problems of adolescents in psychosocial care, including the routes mediating this impact. We obtained data on 315 adolescents, aged 12–18 years, enrolled in child and adolescent social or mental health care. We assessed patient-centered communication by comparing the needs and experiences of adolescents with regard to three aspects of communication: affective quality, information provision, and shared decision-making. Changes in psychosocial problems comprised those reported by adolescents and their parents between baseline and 1 year thereafter. Potential mediators were treatment adherence, improvement of understanding, and improvement in self-confidence. We found a relationship between unmet needs for affective quality, information provision, and shared decision-making and less reduction of psychosocial problems. The association between the unmet need to share in decision-making and less reduction of psychosocial problems were partially mediated by less improvement in self-confidence (30 %). We found no mediators regarding affective quality and information provision. Our findings confirm that patient-centered communication is a major determinant of treatment outcomes in psychosocial care for adolescents. Professionals should be aware that tailoring their communication to individual patients’ needs is vital to the effectiveness of psychosocial care.
- 17 May 2016
- Published by Elsevier in Patient Education and Counseling
- Vol. 99 (11) , 1778-1784
Therapists’ continuations following I don’t know—responses of adolescents in psychotherapy
- 17 May 2016
- Published by Elsevier in Patient Education and Counseling
- Vol. 99 (11) , 1778-1784
Therapists’ continuations following I don’t know—responses of adolescents in psychotherapy
- 8 September 2014
- Published by Wiley in Health Expectations
- Vol. 18 (6) , 2811-2824
Priorities in the communication needs of adolescents with psychosocial problems and their parents
Background: In patient‐centred care, professionals should recognize their patient's needs and adapt their communication accordingly. Studies into patients’ communication needs suggest priorities vary depending on sociodemographic characteristics, and type and severity of the complaints. However, evidence lacks on priorities in the communication needs of adolescents in psychosocial care and their parents.Objective: To assess adolescents’ and parents’ importance ratings concerning affective communication, information provision, shared decision‐making, interprofessional communication and the degree to which client and care characteristics determine these.Methods: Adolescents aged 12–18 (n = 403) and one of their parents (n = 403) rated the importance of communication before the psychosocial care process started. Multivariable logistic regression analysis was applied to determine which characteristics were associated with the 25% lowest importance ratings for communication aspects.Results: Adolescents and parents considered affective communication to be the most important, with shared decision‐making the least important. For adolescents, lower importance ratings were associated with dissatisfaction with prior care (OR 1.8), negative expectations (ORs 1.9–2.4), emotional problems (ORs 0.2–0.5) and low prosocial behaviour skills (ORs 2.0). For parents, low education (ORs 1.7–1.8), negative expectations (OR 0.4), adolescent's hyperactivity/inattention (ORs 0.4–0.5) and low prosocial behaviour skills (ORs 1.8–2.6) determined lower importance ratings.Conclusions: Affective communication has highest priority for adolescents and their parents. Client and care characteristics are associated with client priorities in communication. Being attentive to clients’ educational level, previous care experiences, current expectations and specific problem types might help professionals to adapt better to their clients’ communication needs.
- 8 September 2014
- Published by Wiley in Health Expectations
- Vol. 18 (6) , 2811-2824
Priorities in the communication needs of adolescents with psychosocial problems and their parents
Background: In patient‐centred care, professionals should recognize their patient's needs and adapt their communication accordingly. Studies into patients’ communication needs suggest priorities vary depending on sociodemographic characteristics, and type and severity of the complaints. However, evidence lacks on priorities in the communication needs of adolescents in psychosocial care and their parents.Objective: To assess adolescents’ and parents’ importance ratings concerning affective communication, information provision, shared decision‐making, interprofessional communication and the degree to which client and care characteristics determine these.Methods: Adolescents aged 12–18 (n = 403) and one of their parents (n = 403) rated the importance of communication before the psychosocial care process started. Multivariable logistic regression analysis was applied to determine which characteristics were associated with the 25% lowest importance ratings for communication aspects.Results: Adolescents and parents considered affective communication to be the most important, with shared decision‐making the least important. For adolescents, lower importance ratings were associated with dissatisfaction with prior care (OR 1.8), negative expectations (ORs 1.9–2.4), emotional problems (ORs 0.2–0.5) and low prosocial behaviour skills (ORs 2.0). For parents, low education (ORs 1.7–1.8), negative expectations (OR 0.4), adolescent's hyperactivity/inattention (ORs 0.4–0.5) and low prosocial behaviour skills (ORs 1.8–2.6) determined lower importance ratings.Conclusions: Affective communication has highest priority for adolescents and their parents. Client and care characteristics are associated with client priorities in communication. Being attentive to clients’ educational level, previous care experiences, current expectations and specific problem types might help professionals to adapt better to their clients’ communication needs.