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Family Focused Nursing for Elderly Medical Patients

Family-Focused Nursing for Elderly Medical Patients and Their Family: A Randomized Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02408081
Enrollment
0
Registered
2015-04-03
Start date
2015-04-30
Completion date
2017-01-31
Last updated
2017-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

Depression, Family functioning, Family Focused Nursing, Quality of life

Brief summary

The purpose of this study is to determine whether Family Focused Nursing are effective in the treatment of elderly medical patients with respect to prevalence of depression

Detailed description

Psychosocial issues such as lack of social support and symptoms of depression, are risk factors associated to readmission for elderly medical patients. Families with elderly members in general want to be involved in the caring and want to maintain a close relation to their elderly family member. However, disease in a single family can have a negative effect on all members and may result in dysfunction of the family. International guidelines recommend that the patient's relatives are involved in patient education as well as the treatment. Family interventions might contribute to decline depression and readmissions, besides enhanced quality of life and family function among elderly medical patients and their next of kin.

Interventions

All patients receive treatment as usual. Additionally, patients in the intervention arm receives family focused nursing consultations which are structured as sessions focusing on change, improvement and/or maintenance of family function within cognitive, affective and behavioral knowledge. Each session is organized and individualized according to the wishes and needs for education and counseling of the families within a period of one months.

Sponsors

University Hospital, Gentofte, Copenhagen
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* acute hospitalized * an expected hospitalization of minimum two days * speak and understand Danish * signed informed consent

Exclusion criteria

* dementia (evaluated by the Mini Mental State Examination \[MMSE\] \< 24) * terminally ill patients whose survival rate is assessed to be less than a month

Design outcomes

Primary

MeasureTime frameDescription
Change in depressive symptoms assessed by 9 points measured on the Geriatric Depression ScaleBaseline, 7 days and 6 months after the interventionThe effect of intervention on primary outcome are investigated as longitudinal data at seven days and six month. The data are analysed using mixed models

Secondary

MeasureTime frameDescription
Change in family function score on Brief Family Assessment Measure III7 days and 6 monthsThe effect of intervention on secondary outcome are investigated as longitudinal
Change in health related quality of life on Medical Outcomes Study Short Form, SF-87 days and 6 monthsThe effect of intervention on secondary outcome are investigated as longitudinal
Change in time spent between hospitalization7 days and 6 monthsThe effect of intervention on secondary outcome are investigated as longitudinal

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026