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JOYof ART - an Intervention Study

JOY of ART - an Intervention Study for Older Adults and Their Family Caregivers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03080870
Acronym
JOYofART
Enrollment
120
Registered
2017-03-15
Start date
2017-03-03
Completion date
2018-01-31
Last updated
2017-03-15

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

Conditions

Family Caregivers, Quality of Life

Keywords

Art intervention, Quality of Life, Well-being, Physical performance, Family caregivers, Older adults

Brief summary

Music, dance and visual arts are suggested to support health and well-being of older people. Intervention studies, however, are scarce. JOY of ART study investigates the effects of multicomponent art intervention among older people and ther family caregivers.

Detailed description

JOY of ART study investigates the effects of group based intervention including music, dance and visual arts. Art sessions are provided once a week in three months period each session takes 60 minutes. Eligible participants are recruited from the City of Kuopio, Finland, total 60 dyads, 30 to intervention group and 30 to control group. Health, physical performance and quality of life assessments are conducted at the baseline and in the end of the intervention. In addition, participants are contacted by phone and interviewed six months after the intervention has completed. For family caregivers qualitative interviews are conducted at the baseline and in the end of the study.

Interventions

OTHERArt

Multicomponent art intervention

Sponsors

Kuopio Conservatory
CollaboratorUNKNOWN
Kuopio University Hospital
CollaboratorOTHER
Savonia University of Applied Sciences
CollaboratorOTHER
University of Eastern Finland
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* 65+ age, family caregiving dyad, ability to walk independently or assisted, home dwelling

Exclusion criteria

* severe dementia, severe aphasia

Design outcomes

Primary

MeasureTime frameDescription
Mental Well-being assessed using the Warwick-Edinburgh Mental Well-being scale (WEMWBS)Change in Mental Well-being from baseline until three month follow-upThe Warwick-Edinburgh Mental Well-being scale (WEMWBS)

Secondary

MeasureTime frameDescription
Mobility and Balance assessed using Timed up & Go (TUG)Change in Mobility and Balance from baseline until three month follow-upTimed up & Go (TUG)
Physical Performance assessed using Short Physical Performance Battery (SPPB)Change in Physical Performance from baseline until three month follow-upShort Physical Performance Battery (SPPB)
Quality of Life assessed using EQ- 5D-5LChange in Quality of Life from baseline until three month follow-upEQ- 5D-5L
Psychological Distress assessed using General Health Questionnaire (GHQ 12)Change in Psychological Distress from baseline until three month follow-upGeneral Health Questionnaire (GHQ 12)
Use of Social and Health Care Services assessed using QuestionnaireChange in use of Social and Health Care Service use from baseline until three month follow-upQuestionnaire on Social and Health Care service use

Countries

Finland

Contacts

Primary ContactTarja Välimäki, PhD
tarja.valimaki@uef.fi+358403552267
Backup ContactTimo Lakka, PhD
timo.lakka@uef.fi+358407707329

Outcome results

None listed

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