Abstract
Patients with depression are often dissatisfied with disease- and therapy-related information. The objective of this study was to evaluate an intervention that applied the Common Sense Model to the provision of information during inpatient rehabilitation for patients with depression. The intervention was evaluated in a sequential control group design. Analyses of covariance were used to assess differences between the control and intervention groups. Changes with respect to illness and treatment beliefs (personal control, treatment control, coherence and concerns about medicines), satisfaction with information about medicines, illness and rehabilitation, and depressive burden were selected as primary outcome measures. We observed significant between-group differences indicating the intervention group’s superiority in terms of satisfaction with information regarding medicines. However, the two groups’ changes during rehabilitation did not differ in terms of the other outcomes. The intervention resulted in patients judging that their medication information needs had been more thoroughly fulfilled than those patients who received care-as-usual information. However, the intervention did not prove to be effective when the other outcome variables are considered. Taken together and bearing in mind the limitations of our study—particularly the non-randomised design—our results should be replicated in a randomised controlled trial.
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Acknowledgements
The project “Bedarfsgerechte Patienteninformation auf der Basis subjektiver Konzepte” (Needs-based Patient Information Based on Subjective Concepts) was funded by the German Pension Insurance (Grant No. 0421-FSCP-0544) in the funding priority “Versorgungsnahe Forschung” (Patient-oriented Research). We would like to thank the funders, the cooperating centres Rehabilitationsklinik Frankenhausen DRV-Bund, Bad Frankenhausen; Rehabilitationsklinik “Garder See”, Lohmen; Klinik am Homberg, Bad Wildungen; DE´IGNIS Fachklinik GmbH, Egenhausen; Psychosomatische Fachklinik Schömberg, Schömberg, and the participating patients.
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Manuela Glattacker, Katja Heyduck, Cornelia Meffert, and Teresa Jakob declare that they have no conflict of interests.
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All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation of the Ethics Committee of the University Medical Centre Freiburg and with the Helsinki Declaration of 1975, as revised in 2000. Informed consent was obtained from all patients for being included in the study.
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Glattacker, M., Heyduck, K., Meffert, C. et al. Illness Beliefs, Treatment Beliefs and Information Needs as Starting Points for Patient Information: The Evaluation of an Intervention for Patients with Depression. J Clin Psychol Med Settings 25, 316–333 (2018). https://doi.org/10.1007/s10880-018-9551-1
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DOI: https://doi.org/10.1007/s10880-018-9551-1