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Recruiting NCT05986149

Making Intergenerational Connections Through Arts

Observational Older Adults

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Conversation about arts and culture.
Who it may be relevant to
Registry conditions: Older Adults. Basic parameters: from 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of the study is to evaluate the impact on older adults' wellbeing of participating in a 10-week conversation about arts and culture with an international university student whose native language is not English.

Detailed description

Older adults residing in subsidized housing will participate in a series of online conversations over 10 weeks about various arts and culture with an international university student enrolled at the University of Alabama at Birmingham (UAB); each weekly session will last for about 30 min to one hour.

Participants will complete survey questionnaires before and after the 10-week conversation program, and an exit interview at the end of the conversation program.

Interventions

  • Behavioral Conversation about arts and culture
    intergenerational conversation about arts and culture between older adults and international students who native language is not English.

Primary outcome measures

  • University of California, Los Angeles (UCLA) Loneliness Scale [Time frame: baseline]
  • University of California, Los Angeles (UCLA) Loneliness Scale [Time frame: at 10 weeks]
  • University of California, Los Angeles (UCLA) Loneliness Scale [Time frame: at 2 months]
  • De Jong Gierveld Loneliness Scale [Time frame: baseline]
  • De Jong Gierveld Loneliness Scale [Time frame: at 10 weeks]
  • De Jong Gierveld Loneliness Scale [Time frame: at 2 months]
  • Social Connectedness Scale (SCS) [Time frame: baseline]
  • Social Connectedness Scale (SCS) [Time frame: at 10 weeks]
  • Social Connectedness Scale (SCS) [Time frame: at 2 months]
  • Medical Outcomes Study Social Support Survey (MOSSS) [Time frame: baseline]
Secondary outcome measures (9)
  • Satisfaction with Life Scale (SWLS) [Time frame: baseline]
  • Satisfaction with Life Scale (SWLS) [Time frame: at 10 weeks]
  • Satisfaction with Life Scale (SWLS) [Time frame: at 2 months]
  • Warwick-Edinburgh Mental Well-being Scale (WEMWBS) [Time frame: baseline]
  • Warwick-Edinburgh Mental Well-being Scale (WEMWBS) [Time frame: at 10 weeks]
  • Warwick-Edinburgh Mental Well-being Scale (WEMWBS) [Time frame: at 2 months]
  • Patient Health Questionnaire - 9 items (PHQ-9) [Time frame: baseline]
  • Patient Health Questionnaire - 9 items (PHQ-9) [Time frame: at 10 weeks]
  • Patient Health Questionnaire - 9 items (PHQ-9) [Time frame: at 2 months]

Eligibility criteria

Inclusion criteria

  • Live alone
  • older than 60 years old
  • Residence in a subsidized apartment for at least one year
  • Able to carry on a daily conversation with or without hearing aids
  • Intact cognition as indicated by a score of greater than 5 on the Short Portable Mental Status Questionnaire (SPMSQ)
  • have a working smart phone that can do video-conferencing
  • being able to provide informed consent

Exclusion criteria

  • having physical, or sensory (visual or hearing) deficits or language barriers (non-English communicators) that may impede study participation
  • non-English speaker

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • University of Alabama at Birmingham — Birmingham

Identifiers

NCT: NCT05986149 · IRB-300008546

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗