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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01499797
Other study ID # 2010/403
Secondary ID
Status Completed
Phase N/A
First received October 20, 2011
Last updated June 6, 2013
Start date January 2011
Est. completion date March 2013

Study information

Verified date October 2011
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: ZonMw, Netherlands Organisation for Health Research and Development
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effect of the CareWell-programme on overall functioning of community-dwelling frail elderly persons. Furthermore, the total costs and the cost-effectiveness of the CareWell-programme, in comparison with regular medical care, will be studied.


Recruitment information / eligibility

Status Completed
Enrollment 536
Est. completion date March 2013
Est. primary completion date January 2013
Accepts healthy volunteers No
Gender Both
Age group 70 Years and older
Eligibility Inclusion Criteria:

- Frail community dwelling elderly patients aged 70 years or above. Frailty is determined with a two-phase screening instrument.

Exclusion Criteria:

- Non-frail elders

- Patients in palliative or end-of-life stages of disease

- Patients residing in long-term care facilities (care homes and nursing homes)

- Patients already enrolled in specific dementia-related case-management programmes who lack other health-related problems

- Patients not speaking or understanding the Dutch language

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
The CareWell programme
The CareWell programme contains the following components: multidisciplinary primary care teams working with proactive care plans integrating cure, care and welfare advanced care planning (e.g. recording limitations of treatment, non-resuscitation decisions) medication review case-management guidelines for consultation of in-hospital geriatric experts guidelines for transfers from primary care to home-based facilities and hospital and back practice guidelines for management of common geriatric conditions

Locations

Country Name City State
Netherlands Huisartsengroep Milbergen (van der Ligt/ Krijgsman), Oude Gracht 16 Beek-Ubbergen
Netherlands Gezondheidscentrum de Kroonsteen, Schoolstraat 8 Malden
Netherlands Gezondheidscentrum de Vuursteen, Prinsenweg 6 Molenhoek
Netherlands Gezondheidscentrum Hazenkamp, Vossenlaan 76 Nijmegen
Netherlands Huisartsenpraktijk Danielsplein, Danielsplein 4 Nijmegen
Netherlands Huisartsenpraktijk de Haterse HOED, Couwenbergstraat 34-36 Nijmegen
Netherlands Huisartsenpraktijk Jacobslaan (Dreijerink/ van der Laan-Evers), Jacobslaan 345 Nijmegen
Netherlands Medisch Centrum Brakkenstein, Kanunnik Boenenstraat 8 Nijmegen
Netherlands Medipark (Graat), Hyacinthstraat 3a Uden
Netherlands Huisartsenpraktijk Ubachs/Vogels, Huissteden 1450 Wijchen

Sponsors (6)

Lead Sponsor Collaborator
Radboud University City of Nijmegen, Dutch Healthcare Authority, Health insurances CZ, Health insurances UVIT, ZonMw: The Netherlands Organisation for Health Research and Development

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall functioning Overall functioning is measured with the Katz-15 questionnaire. Katz-15 is embedded in the minimal data set (MDS). This MDS is used by all research projects of the Dutch National Program on Elderly Care 18 months No
Primary Incremental cost-effectiveness ratio (ICER) 18 months No
Secondary Perceived quality of life Perceived quality of life is measured with the RAND-36 questionnaire. RAND-36 is embedded in the minimal data set (MDS). This MDS is used by all research projects of the Dutch National Program on Elderly Care 18 months No
Secondary Psychological well-being Psychological well-being is measured with the RAND-36 questionnaire. 18 months No
Secondary Social functioning Social functioning is measured with the RAND-36 questionnaire. 18 months No
Secondary Perceived health Perceived health is measured with the RAND-36 questionnaire abd Cantril's Self Anchoring Ladder. Both RAND-36 as Cantril's Self Anchoring Ladder are embedded in the minimal data set (MDS). 18 months No
Secondary Utility Utility is measured with the EQ-5D questionnaire. EQ-5D is embedded in the minimal data set (MDS). 18 months No
Secondary Health care consumption Health care consumption including hospital resource consumption, unplanned GP care (evenings, nights and weekends), home care, temporary or permanent admission to a residential care home, temporary or permanent admission to a nursing home, day care, visits to outpatients'clinics. 18 months No
Secondary Use of welfare services 18 months No
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