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Clinical Trial Summary

The researchers' implement and measure the effects of a singing group intervention program for older adults, with an RCT design, in a natural context, on the health, well-being and cognitive function of older adults.


Clinical Trial Description

Background: Singing is a multimodal activity that requires physical, cognitive and psychosocial performance, with benefits in various domains of health and well-being of older adults. In recent years, research has increasingly studied group singing as an important cost-effective intervention to promote active and healthy aging. However, the specific factors responsible for these benefits need further experimental support, as most studies do not allow for causal inferences. This study responds to the need for further randomized controlled trials (RCT), with follow-up measurement, on the benefits of group singing in older adults with diverse socioeconomic status. Also, while most studies often focus on specific outcome measures dimensions, in this study, the conjoint effects of physical, psychosocial, emotional and cognitive dimensions are analyzed, testing mediation and moderation effects of psychosocial and cognitive variables in the health and well-being of the participants. Methods: The team implements and measures the effects of a singing group program for older adults, with an RCT design, in a natural context, before and after the intervention and in a follow-up, four months after the intervention. Participants: 140 retired older adults (> 60 years), users of a social care institution, were invited to participate in a singing group program and randomly allocated to an experimental intervention group (n = 70), and a control (n = 70) group enrolled in the regular activities proposed by the institution. The intervention consists of 34 bi-weekly group singing sessions, of two-hours each, for four months. Measures on social and emotional well-being, cognitive function, and health indicators (as blood pressure, glycemia, cholesterol, c-reactive protein, erythrocyte sedimentation rate, respiratory function, body balance, body activity, sleep quality, medication intake, and health services attendance) will be collected. Interviews on the motivation and perceived benefits of participation will also be collected. Discussion: Significant improvements are expected in the outcome measures in the experimental group after the intervention, in comparison with the control group and the pretest, validating the singing group program as a cost-effective intervention for healthy aging. Psychoemotional, psychosocial and cognitive variables are expected to be mediators of the effects of the program on the health and well-being of the participants. ;


Study Design


Related Conditions & MeSH terms

  • Anxiety
  • Balance
  • Biomarker
  • Blood Glucose
  • Blood Pressure
  • Body Weight
  • C-reactive Protein
  • Cholesterol
  • Cognitive Function
  • Depression
  • Erythrocyte Sedimentation Rate
  • Health Complaint, Subjective
  • Loneliness
  • Medication Compliance
  • Memory
  • Pain Perception
  • Physical Function
  • Quality of Life
  • Respiratory Function
  • Sleep
  • Social Identification
  • Stress
  • Well-Being

NCT number NCT03985917
Study type Interventional
Source Universidade Autónoma de Lisboa
Contact
Status Completed
Phase N/A
Start date December 5, 2018
Completion date February 28, 2020

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