Validierung des FIMA-Fragebogens zur Inanspruchnahme von Versorgungsleistungen anhand von Routinedaten der Krankenversicherung: Welchen Einfluss hat der Erinnerungszeitraum?

Seidl, Hildegard; Hein, Lorenz; Scholz, Stefan; Bowles, David S.; Greiner, Wolfgang; Brettschneider, Christian; König, Hans‐Helmut; Holle, Rolf

doi:10.1055/a-1010-6315

Cited by 14 publications

(12 citation statements)

References 20 publications

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“…The timeline for participants is shown in figure 1. The complete content of collected data with measurement time points is shown in online supplemental tables 1–5 with all related sources reported in the reference list 41–45 54–65…”

Section: Methods and Analysismentioning

confidence: 99%

Encouragement of patients’ self-management in primary care for the prevention of cardiovascular diseases (DECADE): protocol for a cluster randomised controlled trial

et al. 2023

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IntroductionCardiovascular diseases are the most common cause of death in Germany and among the most frequent reasons for encounters in primary care. Most patients with cardiovascular risks (CVRs) have difficulties implementing health-promoting behavioural changes. In this study, a complex intervention containing evidence-based patient materials and structured follow-up consultations are intended to strengthen patients’ self-management to improve health behaviour.Methods and analysisIn this cluster randomised controlled trial, we investigate the effects of the intervention "Decision aid, action planning and follow-up support for patients to reduce the 10-year risk of cardiovascular diseases" (DECADE) using a 2×2 design. All patients, including the control group (CG), receive a CVR calculation. Three intervention groups (IGs) receive one or both of two different components of the DECADE intervention: IG1 (patient materials), IG2 (follow-up consultations) and IG3 (patient materials and follow-up consultations). The study was planned to be conducted with 77 general practitioners in 3 German regions and a target sample size of 924 patients. The observation period for each patient amounts to 12 months with three patient surveys: baseline (t0), after 6 and 12 months (t1 and t2). The primary outcome is patient activation (Patient Activation Measure 13 (PAM13-D)) at t1. Secondary outcomes include PAM13-D at t2 and further patient-reported and clinical outcomes at t1 and t2. We will also analyse the cost-effectiveness of the intervention, the degree of usage and satisfaction with the intervention.Ethics and disseminationThe study was first approved by the lead ethics committee of the University of Freiburg on 15 April 2021 (vote number: 21-1078) and subsequently by the other ethics committees in the study regions (Ethics committee of medical association Baden-Württemberg (B-F-2021-078), Ethics Committee of the Technische Universität Dresden, Dresden (BO-EK-251052021), Ethics Committee of the State Chamber of Physicians of Saxony (EK-BR-92/21-1), Ethics Committee of the Hamburg Medical Association (2021-200013-BO-bet)). Informed consent is required for patients to participate in the study. The results of this study will be published in peer-reviewed journals and presented at congresses by the DECADE team. The DECADE lead management will communicate the results to the funder of this study.Trial registration numberGerman Clinical Trials Register, DRKS00025401 (registration date: 21 June 2021); International Clinical Trials Registry Platform, DRKS00025401.

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Section: Methods and Analysismentioning

confidence: 99%

Encouragement of patients’ self-management in primary care for the prevention of cardiovascular diseases (DECADE): protocol for a cluster randomised controlled trial

et al. 2023

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“…Health-related resource use in an elderly population Healthcare resource utilisation and medication will be assessed using the validated 'Questionnaire for Health-Related Resource Use in an Elderly Population' (Fragebogen zur Inanspruchnahme medizinischer und nicht-medizinischer Versorgungsleistungen im Alter). It consists of 14 items and is a valid tool to determine health related resource use in older population [43].…”

Section: European Quality Of Life Five-dimension Five-level Scalementioning

confidence: 99%

Effectiveness of an evidence-based care pathway to improve mobility and participation in older patients with vertigo and balance disorders in primary care (MobilE-PHY2): study protocol for a multicentre cluster-randomised controlled trial

Horstmannshoff

Skudlik

Petermann

et al. 2023

Trials

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Background Vertigo, dizziness or balance disorders (VDB) are common leading symptoms in older people, which can have a negative impact on their mobility and participation in daily live, yet, diagnosis is challenging and specific treatment is often insufficient. An evidence-based, multidisciplinary care pathway (CPW) in primary care was developed and pilot tested in a previous study. The aim of the present study is to evaluate the effectiveness and safety of the CPW in terms of improving mobility and participation in community-dwelling older people with VDB in primary care. Methods For this multicentre cluster randomised controlled clinic trial, general practitioners (GP) will be recruited in two regions of Germany. A total of 120 patients over 60 years old with VDB will be included. The intervention is an algorithmized CPW. GPs receive a checklist for standardise clinical decision making regarding diagnostic screening and treatment of VDB. Physiotherapists (PT) receive a decision tree for evidence-based physiotherapeutic clinical reasoning and treatment of VDB. Implementation strategies comprises educational trainings as well as a workshop to give a platform for exchange for the GPs and PTs, an information meeting and a pocket card for home care nurses and informal caregivers and telephone peer counselling to give all participants the capability, opportunity and the motivation to apply the intervention. In order to ensure an optimised usual care in the control group, GPs get an information meeting addressing the national guideline. The primary outcome is the impact of VDB on participation and mobility of patients after 6 month follow-up, assessed using the Dizziness Handicap Inventory (DHI) questionnaire. Secondary outcomes are physical activity, static and dynamic balance, falls and fear of falling as well as quality of life. We will also evaluate safety and health economic aspects of the intervention. Behavioural changes of the participants as well as barriers, facilitating factors and mechanisms of impact of the implementation will be investigated with a comprehensive process evaluation in a mixed-methods design. Discussion With our results, we aim to improve evidence-based health care of community-dwelling older people with VDB in primary care. Trial registration DRKS, DRKS00028524 retrospectively registered on March 24, 2022.

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“…To assess costs, health care utilization will be measured by selected questions from the questionnaires FIMA (69) and FIMPsy (70). To calculate costs, the measured health care utilization will be monetarily valued using standardised unit costs for Germany (71,72).…”

Section: Cost Effectivenessmentioning

confidence: 99%

Internet based versus face-to-face transdiagnostic treatment for emotional disorders in Arabic- and Farsi-speaking refugees: Study protocol of a three-arm randomized controlled non-inferiority trial.

Boettcher

Heinrich

Boettche

et al. 2023

Preprint

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Background Refugee populations have an increased risk for mental disorders, such as depressive, anxiety, and posttraumatic stress disorders. Comorbidity is common. At the same time, refugees face multiple barriers to accessing mental health treatment. Only a minority of them receives adequate help. The planned trial evaluates a low-threshold, transdiagnostic Internet based treatment. The trial aims at establishing its efficacy and cost-effectiveness compared with face-to-face treatment and no treatment. Methods In a three-arm, multi-site randomized-controlled trial we will test the non-inferiority of the Internet based, cognitive-behavioral treatment to content-equivalent face-to-face treatment and its superiority to waitlist control. N = 499 treatment-seeking Arabic- or Farsi-speaking patients, meeting diagnostic criteria for a depressive, anxiety, and/or posttraumatic stress disorder will be randomized to one of three groups. The first group receives an Internet based treatment with weekly written guidance provided by Arabic- or Farsi-speaking professionals. The second group will receive weekly face-to-face treatment provided by German-speaking CBT therapists and facilitated by interpreters. The third group will wait for three months and then receive their treatment of choice. Both active treatments are based on the Common Elements Treatment Approach (CETA), are tailored to the individual patient, and take 6–16 weeks. Discussion The planned trial will result in an estimate of the (comparative) efficacy of two valuable treatment options for the most common mental disorders in refugees. Trial registration The trial was registered at GCTR, the German clinical trials register, as DRKS00024154 on 2021-02-01.

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Validierung des FIMA-Fragebogens zur Inanspruchnahme von Versorgungsleistungen anhand von Routinedaten der Krankenversicherung: Welchen Einfluss hat der Erinnerungszeitraum?

Cited by 14 publications

References 20 publications

Encouragement of patients’ self-management in primary care for the prevention of cardiovascular diseases (DECADE): protocol for a cluster randomised controlled trial

Encouragement of patients’ self-management in primary care for the prevention of cardiovascular diseases (DECADE): protocol for a cluster randomised controlled trial

Effectiveness of an evidence-based care pathway to improve mobility and participation in older patients with vertigo and balance disorders in primary care (MobilE-PHY2): study protocol for a multicentre cluster-randomised controlled trial

Internet based versus face-to-face transdiagnostic treatment for emotional disorders in Arabic- and Farsi-speaking refugees: Study protocol of a three-arm randomized controlled non-inferiority trial.

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