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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01841853
Other study ID # Livslots Angered
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2012
Est. completion date January 2016

Study information

Verified date May 2019
Source Göteborg University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overarching aim with this study was to develop, implement and evaluate a health promoting programme for people from Finland or the Western Balkan region, who were 70 years of age or older and independent daily activites (1). The aim of the programme was to prevent or delay dependence in daily activities, health decline, and frailty. The study focused on both evaluation and implementation and the data collection finished in 2016


Description:

The study has developed tools for collaboration between the target group, staff and researchers, as well as with tools to bridge barriers to health promotion. For example, alternative ways to recruit participants and to collect and analyse data in studies with and for people who are ageing in a migration context.

The findings describe how a person-centred approach could be used to make use of the resources of the target groups, and visualise methods to bridge linguistic barriers. The education material from Older people in the risk zone has also been translated to Bosnian Serbo-Croatian and Finnish.


Recruitment information / eligibility

Status Completed
Enrollment 131
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria:

- Foreign-born from Finland or any of five countries in the Western Balkans (Bosnia-Herzegovina, Croatia, Macedonia, Montenegro, and Serbia)

- 70 years of age or older

- Living in Angered, Gothenburg

- Living in their ordinary housing

- Not dependent on informal or formal help in daily activities

Exclusion Criteria:

- Impaired cognition, Mini Mental State Examination (MMSE) below 80% of administered items

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Senior meetings
The intervention will be led by professionals such as a registered occupational therapist, a nurse, a physical therapist, and a social worker. The intervention will comprise four weekly meetings in small groups (4-6 participants) in addition to an individual follow-up home visit two to three weeks after the last senior meeting. To use groups involve the possibility of peer education where participants in a person-centeredness perspective are seen as experts on their own situation and learn from each other. The relationship between the personnel and the participants in the senior meetings can be described as a partnership. Respect for the participant and his/her values, and that the participant gets an opportunity to maintain and develop their own power over their own everyday activities will be essential in the meeting.

Locations

Country Name City State
Sweden Synneve Dahlin-Ivanoff Gothenburg

Sponsors (2)

Lead Sponsor Collaborator
Göteborg University The Swedish Research Council

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Activities of Daily Life (ADL) The ADL-staircase change from baseline at 6 months and 1 year
Primary Change of Sense of Coherence (KASAM) KASAM (by Antonovsky) change from basline at 6 months and 1 year
Secondary Change of Fatigue The Mob-T scale baseline, 6 months, and 1 year
Secondary Change of Grip strength North Coast-dynamometer baseline, 6 months, and 1 year
Secondary Change of Physical activity Questionnaire and Physical and domestic activity scale basline, 6 months, and 1 year
Secondary Change of Balance The balance scale basline, 6 months, and 1 year
Secondary Change of Gait speed Four-meter walking test basline, 6 months, and 1 year
Secondary Change of Weight loss The Göteborg Quality of Life Instrument basline, 6 months, and 1 year
Secondary Change of Cognition Mini Mental State Examination (MMSE) basline, 6 months, and 1 year
Secondary Change of Visual impairment KM-visual acuity chart basline, 6 months, and 1 year
Secondary Change of Falls Questionnaire basline, 6 months, and 1 year
Secondary Change of Fear of falls FES-I baseline, 6 months, 1 year
Secondary Change of Illness CIRS-G Baline, 6 months, and 1 year
Secondary Change of Symptoms The Göteborg Quality of Life Instrument Basline, 6 months, and 1 year
Secondary Change of Change of Depression GDS 20 Baseline, 6 months, and 1 year
Secondary Health-care consumption Register data Baseline, 6 months, and 1 year
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