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Dive into the research topics where Froukje Boersma is active.

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Featured researches published by Froukje Boersma.


Dementia and Geriatric Cognitive Disorders | 2010

Review of Effects of Physical Activity on Strength, Balance, Mobility and ADL Performance in Elderly Subjects with Dementia

Christiaan G. Blankevoort; Marieke J. G. van Heuvelen; Froukje Boersma; Helga Luning; Jeltsje de Jong; E.J.A. Scherder

Background/Aims: Elderly individuals with dementia are vulnerable for a decline in physical functioning and basic activities of daily living (BADL) which can lead to a decline in autonomy and participation. This study reviews the effect of physical activity on physical functioning and BADL in elderly subjects with dementia. Methods: A systematic search of the literature was performed. Key words related to the elderly, dementia, exercise interventions and physical outcome measures were used. Results: Sixteen studies were included. It was found that physical activity was beneficial in all stages of dementia. Multicomponent interventions (e.g. a combination of endurance, strength and balance) led to larger improvements in gait speed, functional mobility and balance, compared to progressive resistance training alone. BADL and endurance improved but were only assessed in multicomponent interventions. Lower-limb strength improved equally in multicomponent interventions and progressive resistance training. Conclusion: Multicomponent interventions can improve physical functioning and BADL in elderly subjects regardless of the stage of dementia. The best results were obtained in the interventions with the largest training volume. However, the small number of high-quality studies, and heterogeneity of the participants and interventions prevent us from drawing firm conclusions. Recommendations are given with respect to methodological issues, further research and practical guidelines.


Journal of Clinical Pharmacy and Therapeutics | 2007

A study of medication reviews to identify drug-related problems of polypharmacy patients in the Dutch nursing home setting

F. Finkers; Jan Gerard Maring; Froukje Boersma; Katja Taxis

Background:  Little is known about the extent of drug‐related problems of polypharmacy patients in Dutch nursing homes.


International Journal of Geriatric Psychiatry | 2013

The effect of music therapy compared with general recreational activities in reducing agitation in people with dementia: a randomised controlled trial

Annemiek Vink; Marij Zuidersma; Froukje Boersma; P. de Jonge; Sytse U. Zuidema; Joris P. J. Slaets

This study aimed to compare the effects of music therapy with general recreational day activities in reducing agitation in people with dementia, residing in nursing home facilities.


Dementia and geriatric cognitive disorders extra | 2012

Recommended measures for the assessment of cognitive and physical performance in older patients with dementia: a systematic review

Willem J. R. Bossers; Lucas H. V. van der Woude; Froukje Boersma; E.J.A. Scherder; Marieke J. G. van Heuvelen

Aim/Goal: To recommend a set of neuropsychological and physical exercise tests for researchers to assess cognition and physical fitness in clinical trials with older patients with dementia; to create consensus, decrease heterogeneity, and improve research quality. Methods: A literature search (2005–2011) yielded 89 randomized controlled trials. To provide information on test recommendations the frequency of test use, effect size of the test outcome, study quality, and psychometric properties of tests were analyzed. Results: Fifty-nine neuropsychological tests (cognitive domains: global cognition, executive functioning, memory, and attention) and 10 exercise tests (physical domains: endurance capacity, muscle strength, balance, and mobility) were found. Conclusion: The Severe Impairment Battery, Mini Mental State Examination, and Alzheimer Disease Assessment Scale – cognitive subscale were recommended to measure global cognition. The Verbal Fluency Test Category/Letters, Clock Drawing Test, and Trail Making Test-B were recommended to measure executive functioning. No specific memory test could be recommended. The Digit Span Forward, Digit Span Backward, and Trail Making Test-A were recommended to measure attention. As physical exercise tests, the Timed Up and Go and Six Meter Walk for mobility, the Six Minute Walk Distance for endurance capacity, and the Tinetti Balance Scale were recommended.


Journal of Clinical Epidemiology | 1998

Prevalence of Dementia in a Rural Netherlands Population and the Influence of DSM-III-R and CAMDEX Criteria for the Prevalence of Mild and More Severe Forms

Froukje Boersma; Jan A. Eefsting; Wim van den Brink; Maarten W. J. Koeter; Willem van Tilburg

To obtain estimates of the prevalence of mild and moderate/severe dementia among people age 65 and over, applying criteria for severity of both DSM-III-R and CAMDEX, a two-stage community-based study was conducted in a rural area of the Netherlands. In the first stage, 2191 subjects (out of the target population of 2655) participated in an interview which included the Mini-Mental State Examination (MMSE). Based on MMSE score, a non-proportional random sample (n=496) was drawn for the second stage. A total of 421 subjects responded and were subsequently examined using the Cambridge Examination for Mental Disorders of the Elderly (CAMDEX). In determining the severity of dementia, criteria of both DSM-III-R and CAMDEX were applied. Overall prevalence for both classification systems was 6.5%. There was a large discrepancy between the two classification systems with regard to the criteria for rating severity. The prevalence of moderate/severe dementia using DSM-III-R criteria was twice as high as the prevalence using CAMDEX criteria. These findings reflect the differences between DSM-III-R and CAMDEX in descriptions of dementia severity. Rating according to CAMDEX predicts institutionalization in specialized nursing homes somewhat better than staging according to DSM-III-R. Both content analysis and institutionalization data suggest that the CAMDEX operationalization of rating severity seems preferable.


PLOS ONE | 2014

Feasibility of a Combined Aerobic and Strength Training Program and Its Effects on Cognitive and Physical Function in Institutionalized Dementia Patients. A Pilot Study

Willem J. R. Bossers; E.J.A. Scherder; Froukje Boersma; Tibor Hortobágyi; Lucas H. V. van der Woude; Marieke J. G. van Heuvelen

Objectives We examined the feasibility of a combined aerobic and strength training program in institutionalized dementia patients and studied the effects on cognitive and physical function. Methods Thirty-three patients with dementia, recruited from one nursing home, participated in this non-randomized pilot study (25 women; age = 85.2±4.9 years; Mini Mental State Examination = 16.8±4.0). In phase 1 of the study, seventeen patients in the Exercise group (EG) received a combined aerobic and strength training program for six weeks, five times per week, 30 minutes per session, in an individually supervised format and successfully concluded the pre and posttests. In phase 2 of the study, sixteen patients in the Social group (SG) received social visits at the same frequency, duration, and format and successfully concluded the pre and posttests. Results Indices of feasibility showed that the recruitment and adherence rate, respectively were 46.2% and 86.3%. All EG patients completed the exercise program according to protocol without adverse events. After the six-week program, no significant differences on cognitive function tests were found between the EG and SG. There was a moderate effect size in favor for the EG for the Visual Memory Span Forward; a visual attention test. There were significant differences between groups in favor for the EG with moderate to large effects for the physical tests Walking Speed (p = .003), Six-Minute Walk Test (p = .031), and isometric quadriceps strength (p = .012). Conclusions The present pilot study showed that it is feasible to conduct a combined aerobic and strength training program in institutionalized patients with dementia. The selective cognitive visual attention improvements and more robust changes in motor function in favor of EG vs. SG could serve as a basis for large randomized clinical trials. Trial Registration trialregister.nl 1230


Reviews in The Neurosciences | 2007

Physical activity and cognition in Alzheimer's disease: Relationship to vascular risk factors, executive functions and gait

E.J.A. Scherder; Laura Eggermont; Joseph A. Sergeant; Froukje Boersma

Epidemiological studies show a positive relationship between physical activity and cognition in patients with Alzheimers disease (AD). A relatively small number of intervention studies have examined the effects of physical activity, such as walking, on cognition in AD patients. The results of these studies, reviewed here, include both positive and negative findings. The finding that physical activity does not improve cognition in all AD patients could be explained by two factors that have received little attention thus far: executive dysfunction and gait disturbances. These two factors are part of a cascade of events, initiated by cerebrovascular disease in AD. This cascade of events is addressed in detail. Finally, (non)pharmacological interventions to improve executive dysfunctions and gait disturbances in patients with AD are discussed.


International Journal of Geriatric Psychiatry | 1997

Care Services for Dementia Patients: Predictors For Service Utilization

Froukje Boersma; Jan A. Eefsting; Wim van den Brink; Willem van Tilburg

Aim. The objective of this study was to examine service utilization figures among a representative sample of demented patients and to determine whether sociodemographic and health‐related variables are associated with care utilization.


International Journal of Geriatric Psychiatry | 2015

Development of a practice guideline for optimal symptom relief for patients with pneumonia and dementia in nursing homes using a Delphi study

Tessa van der Maaden; Jenny T. van der Steen; Henrica C.W. de Vet; Wilco P. Achterberg; Froukje Boersma; J.M.G.A. Schols; Jos F. J. M. van Berkel; David R. Mehr; Marcel Arcand; Andy I. M. Hoepelman; Raymond T. C. M. Koopmans; C.M.P.M. Hertogh

This study aimed to develop a practice guideline for a structured and consensus‐based approach to relieve symptoms of pneumonia in patients with dementia in nursing homes.


BMJ Open | 2014

Discontinuing inappropriate medication in nursing home residents (DIM-NHR Study): protocol of a cluster randomised controlled trial.

Hans Wouters; Elise H. Quik; Froukje Boersma; Peder Nygård; Judith Bosman; Wendelien M Böttger; Hans Mulder; Jan-Gerard Maring; Linda Wijma-Vos; Tim Beerden; Jasperien van Doormaal; Maarten Postma; Sytse U. Zuidema; Katja Taxis

Introduction Nursing home residents often have a high number of comorbidities resulting in polypharmacy. Inappropriate prescribing is therefore likely to occur, which in turn is expected to worsen cognitive impairment, to increase the fall risk and to decrease residents’ quality of life. The objective of the ‘Discontinuing Inappropriate Medication in Nursing Home Residents’ (DIM-NHR) study is to examine the efficacy and cost-effectiveness of the Multidisciplinary Multistep Medication Review (3MR) that is aimed at optimising prescribing and discontinuing inappropriate medication. Methods A cluster randomised controlled trial will be conducted. Elderly care physicians and their wards (clusters) will be randomised. Data will be collected at baseline and 4 months after the 3MR has taken place. Six hundred nursing home residents will be recruited of whom more than half are expected to suffer from dementia. The 3MR will be based on consensus criteria and the relevant literature and will be performed by the patient’s elderly care physician in collaboration with a pharmacist. Analysis Primary outcomes—the difference in proportion of residents who successfully discontinued inappropriate medication between the intervention and control group at follow-up. Secondary outcomes—undertreatment, exposure to anticholinergic and sedative medicines, neuropsychiatric symptoms, cognitive function, falls, hospital admission, quality of life and cost-effectiveness. Ethics and dissemination Participant burden will be kept at a minimum. The elderly care physician will remain free to adjust medication when symptoms relapse or adverse events occur, rendering serious adverse events highly unlikely. Study findings will be published in peer-reviewed journals and a 3MR toolkit will be developed. Trial registration number This study has been registered at http://www.ClinicalTrials.gov (trial registration number: NCT01876095)

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Katja Taxis

University of Groningen

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Sytse U. Zuidema

University Medical Center Groningen

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Marieke J. G. van Heuvelen

University Medical Center Groningen

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Willem J. R. Bossers

University Medical Center Groningen

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Hans Wouters

University of Groningen

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Jan A. Eefsting

VU University Medical Center

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Lucas H. V. van der Woude

University Medical Center Groningen

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Joris P. J. Slaets

University Medical Center Groningen

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Marij Zuidersma

University Medical Center Groningen

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