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Volunteer contact: A randomized controlled trial on the effectiveness of an individual life-review intervention for frail people of 65 years and older

Volunteer contact: A randomized controlled trial on the effectiveness of an individual life-review intervention for frail people of 65 years and older - Volunteer contact

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON41500
Enrollment
134
Registered
2013-07-23
Start date
2013-04-25
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

welbevinden happiness well-being

Interventions

'Dear memories' trains participants to retrieve specific, positive memories. The intervention consists of five structured conversations of 45 minutes each, in which trained volunteers ask questions

Sponsors

Universiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. An age of 65 years or older and receiving health within a healthcare organization (by receiving outpatient or home care, or living in a care or nursing home); 2. Lowered well-being (score of 4.8or lower on Mental Health Conntinuum Short Form)

Exclusion criteria

Exclusion criteria: 1. Severe cognitive impairment, measured by a score of 18 or lower on the Mini Mental State Examination (MMSE, Folstein et al 1975); 2. The diagnosis of major depressive episode (based on the MINI, 8 or 9 of the 9 DSM-IV symptoms of depression); 3. Having started with medication for depressive symptoms within the past 3 months; 4. Poor command of the Dutch language.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is promotion of well-being as measured with the Mental Health Continuum Short Form. Well-being will be measured at baseline and 2 and 8 months after baseline.

Secondary

MeasureTime frame
The secondary outcomes will be measured at baseline and 2 and 8 months after basline: improvement in (or not developing a) depressive episode (only at baseline and 8 months after baseline), and mastery, and a reduction in depressive symptoms, anxiety symptoms, and loneliness .

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)