Prevention of loneliness and depression in elderly nursing home patients living in Amsterdam using life review therapy

ISRCTN ISRCTN21151711
DOI https://doi.org/10.1186/ISRCTN21151711
Protocol serial number N/A
Sponsor VU University Medical Centre (The Netherlands)
Funder Stichting Nuts Ohra (The Netherlands)
Submission date
01/02/2007
Registration date
01/02/2007
Last edited
01/02/2007
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Bas Steunenberg
Scientific

VU University Medical Center
Department of Clinical Psychology
Van der Boechorststraat 1
Amsterdam
1081 BT
Netherlands

Phone +31 (0)20 598 8703
Email B.Steunenberg@psy.vu.nl

Study information

Primary study designInterventional
Study designRandomised controlled, parallel group trial
Secondary study designRandomised controlled trial
Scientific title
Study objectivesLife review therapy will have a positive effect on the level of depressive symptoms of nursing home inhabitants.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedDepressive symptoms
InterventionIntervention:
The life review consisted of autobiographical retrieval practice that entailed focusing on a particular life period each week - childhood, adolescence, adulthood, and summary. For each period 14 quesions were asked that were designed to prompt specific memories. Examples of questions include ''What did your mother or father do one day when you were a child that astonished you?''.

Intervention sessions were tape-recorded and were scored by a psychologist. At pre- and post-test the following questionnaires were administered:
1. Depressive symptoms (eight-item Geriatric Depression Scale [GDS-8])
2. Cognitive functioning (Mini Mental State Examination [MMSE])
3. Mini International Neuropsychiatric Interview (MINI) (Diagnostic and Statistical Manual of mental disorders [DSM] diagnoses depression and dysthymia)
4. Anxiety (Hamilton Anxiety and Depression Scale [HADS])
5. Loneliness (De Jong Gierveld Loneliness Scale)
6. Autobiographical Memory Test (AMT)
7. Worrying (Penn State Worry Questionnaire [PSWQ])
8. Neuroticism (Neuroticism-Extraversion-Openness Five-Factor Inventory [NEO-FFI]-subscale)
9. Quality of life (Dutch Scale for Subjective well-being of the elderly [SSWO], short Portable Mental Status (PMS) questionnaire, ''balans opmaken vragenlijst'')

Control:
Waiting list (after three months).
Intervention typeOther
Primary outcome measure(s)

1. Depression (GDS-8, MINI-interview) and loneliness (De Jong Gierveld Loneliness Scale)
2. Anxiety, HADS, autobiographical memory (AMT)

Post-treatment one or two weeks after ending intervention (four weeks after inclusion).

Key secondary outcome measure(s)

Analysing the influence of covariates on the outcome of the life review therapy (neuroticism [NEO-FFI], worrying [PSWQ-11], quality of life)/mastery (PMS).

Completion date01/08/2007

Eligibility

Participant type(s)Patient
Age groupSenior
SexAll
Target sample size at registration100
Key inclusion criteria1. Aged over 65
2. Living in a nursing home
3. Normal cognitive functioning/no signs of dementia
4. No pharmacological treatment
Key exclusion criteria1. No or less depressive symptoms
2. Mild or severe cognitive symptoms
Date of first enrolment01/02/2007
Date of final enrolment01/08/2007

Locations

Countries of recruitment

  • Netherlands

Study participating centre

VU University Medical Center
Amsterdam
1081 BT
Netherlands

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan