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Singing Groups for Seniors: Well-Being, Cognitive Function and Health (Sing4Health)

Primary Purpose

Cognitive Function, Well-Being, Physical Function

Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Singing Group Intervention Program
Alternative Social and Leisure Activities
Sponsored by
Iolanda Costa Galinha
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cognitive Function focused on measuring Singing Group, Choir, Intervention, Older Adults, Well-Being, Cognitive Function, General Health

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion criteria:

  • Being 60 years old or older;
  • Retired;
  • Accept the invitation to participate in the singing group program;
  • Not having participated in other intervention programs in the previous four months.

Exclusion criteria:

  • Having a severe impairment, that is disabling for the participation in the singing group activity (e.g. severe cognitive, auditory, visual or mobility impairments).

Sites / Locations

  • Universidade Autónoma de Lisboa

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention Singing Group Program

Alternative Social and Leisure Activities

Arm Description

Singing group intervention program that includes six components: (1) vocal warm-up exercises; (2) vocal technique; (3) rehearsal of repertoire; (4) break for socialization; (5) creation and presentation of a show; (6) assessment of participants performance (vocal tuning).

While the experimental group is participating in the intervention program, the control group will participate in the other activities proposed by the day care centers, which will be registered.

Outcomes

Primary Outcome Measures

Quality of Life - WHOQOL-BREF
The WHOQOL-BREF measures the subjective perception of quality of life. It consists of 26 items, of which two items measure global quality of life and 24 items measure four dimensions. In this study the (1) Physical health, (2) Psychological Health, (3) Social relationships will be measured. The items are answered in a 5 point scale, from 1 (Very Bad; Very Unsatisfied; Nothing; Never) to 5 (Very Good; Very Satisfied; Extremely; Always).
Quality of Life - WHOQOL-OLD
The WHOQOL-OLD measures the quality of life specifically for older adults, with 28 items, measuring six dimensions. In this study the dimensions (1) sensory abilities; (2) autonomy; (3) past, present, and future activities; and (4) social participation will be measured. The items are answered in a 5-point scale, from 1 (Nothing; Very Bad; Very Unsatisfied) to 5 (Extremely; Very Good; Very Satisfied).
Depression, Anxiety and Stress - Dass 21
The DASS 21 measures Anxiety, Depression and Stress. Consists of 21 items distributed in 3 subscales of 7 items each, answered on a 4-point scale, ranging from: 0 "It did not apply to me", to 3 "Applied to me most of the time".
Positive and Negative Affect - PANAS
Measures the frequency of positive and negative emotions, during the past four months, and consists of two scales with 10 items each, answered on a 5-point scale from: 1 "nothing or very slightly"; to 5 "extremely".
Life Satisfaction - SWLS
Measures satisfaction with life in general, according to the persons' criteria. Consists of five items, answered on a 5-point scale from: 1 = strongly disagree; to 5 - I agree very much.
Self-Esteem - RSES
Measures the appreciation of self-worth and self-acceptance, with 10 items, answered on a 4-point Likert scale, from: 1 = strongly disagree; to 4 = strongly agree.
Loneliness - UCLA Loneliness Scale
Measures the feeling of being cut off from others, with four items, derived from the longer version of the ULS-20, answered on a 4-point scale from: 0 (Never), to 4 (Often / Many Times).
Social Identification - FISI
Measures the emotional evaluation of the relationship between the self and the ingroup, with four items, answered on a 7-point scale, ranging from: 1 "strongly disagree", to 7 "strongly agree".
Social Well-Being - Scale of Social Well-Being
Measures a multidimensional construct of social well-being including the dimensions: social acceptance, social coherence, social actualization, social integration and social contribution. Constituted by 33 items, answered on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree).
Cognitive Function - MoCA
Measures six cognitive functions: executive function; visuospatial skills; short-term memory; language; attention, concentration and working memory; and temporal and spatial orientation. The test is constituted by six groups of tasks and exercises. The maximum score is 30 points; higher scores indicate better cognitive performance.
Short-term auditory verbal memory - RAVELT
The scale measures the rate of verbal learning, learning strategies, retroactive, and proactive interference, presence of confabulation or confusion in memory processes, retention of information, and differences between learning and retrieval. It consists of a list of 15 unrelated words repeated over five different trials, which participants are asked to repeat.
Attention and Executive Function - Trail Making Test
The test measures the processing speed, mental flexibility, and divided attention. It consists of a task of connecting a trail of numbers with a drawing line. In this study, TMT A will be used, providing two direct scores: time to complete part A and performance errors.
Processing Speed - Digit Symbol Test
The test measures the processing speed of non-verbal information. It consists of a task of drawing figures corresponding to numbers. It also measures cognitive and motor speed, planning ability, visual memory, visuomotor coordination, motivation to perform the task and attention.
Blood Pressure - Licensed laboratory
Measures the pressure with which the blood circulates within the arteries. Data collected and analyzed by a licensed laboratory.
Pulse - Licensed laboratory
The count of arterial pulse per minute, measures the number of times the heart beats per minute. Data collected and analyzed by a licensed laboratory.
Glycemia - Blood sample - Licensed laboratory
Measures the amount of glucose present in the blood, used in the diagnosis and treatment of several diseases as diabetes mellitus or hypoglycemia. Data is collected and analyzed by a licensed laboratory.
Cholesterol - Blood sample - Licensed laboratory
Measures total cholesterol, a fatty substance produced by the liver, present in all body cells and essential for the formation of the cell membranes hormone synthesis, digestion of fats, production of bile, metabolism of vitamins A, D, E and K, important in the constitution of global coronary disease risk. Data is collected and analyzed by a licensed laboratory.
C-reactive protein (CRP) - Blood sample - Licensed laboratory
Measures C-reactive protein, a protein produced in the liver and in case of inflammatory states its production increases. Indicates an ongoing, but not specific, organism infection. It can also be high in case of neoplasia. Data collected and analyzed by a licensed laboratory.
Erythrocyte Sedimentation Rate (ESR) - Blood sample - Licensed laboratory
A measure of the red blood cells sedimentation by micro photometry over a period of time. A blood sedimentation rate is tested to detect inflammation in the body or to follow the progress of a disease. Data is collected and analyzed by a licensed laboratory.
Body Weight - Professional scale
Body weight is assessed by weighing the person with light clothing, without shoes and while fasting.
Respiratory Function - Spirometry (Medikro Pro) - Air Volume
The test consists of a simple examination, which allows to globally evaluate how the lungs are functioning by measuring the volume of air (measured in litres with the tests FVC, FEV1 and FEV6). In addition the Tiffeneau-Pinelli Index will be measured, which is a ratio between FVC and FEV1. Data is collected by trained researchers in motricity sciences.
Respiratory Function - Spirometry (Medikro Pro) - Air Speed
The test consists of a simple examination, which allows to globally evaluate how the lungs are functioning by measuring the speed of air expired (litres per second, measured with the tests PEF, FEF 25 to 75%). Data is collected by trained researchers in motricity sciences.
Body Balance - Unipedal Stance Test.
The participant is instructed to balance on a foot of their choosing for up to 20 seconds. The number of seconds in balance is registered as the score of this test. Data collected by trained researchers in motricity sciences.
Physical Activity - Actigraphy (GT3X accelerometer)
Actigraphy registers the body accelerations in three axes (vertical, antero-posterior, and medio-lateral). Participants will be asked to wear the accelerometer around the hip for seven consecutive days (day and night, except when bathing). The accelerometer provides a measure of the frequency, intensity, and duration of physical activity and allows for the classification of activity levels as sedentary, light, moderate and vigorous.
Sleep Quality - Actigraphy (GT3X accelerometer)
Actigraphy registers the body accelerations in three axes (vertical, antero-posterior, and medio-lateral). Participants will be asked to wear the accelerometer around the hip for seven consecutive days (day and night, except for bathing). The accelerometer provides a measure of the frequency, intensity, and duration of physical activity and allows for a measure of the total duration of sleep.
Pain Perception - The Brief Pain Inventory,
The scale measures different types of pain, with nine questions: a first one that is optional; a second one based on drawings of the human body to locate the pain in the body; four items about pain intensity (worst pain, least pain, average pain, pain right now); two items on pain relief or medication; and one item on pain interference, with seven sub-items (general activity, mood, walking ability, normal walk, relations with other people, sleep, and enjoyment of life). Answering options from: 0 "No pain / Did not interfered"; and 10 "The greatest pain possible / Completely interfered".
Medication Intake - Social Support Institution
Medication and dosage are registered and supplied by the Social Care Institution to the research team with the authorization of the participants.
Health Services Attendance - Social Support Institution
Number and type of health services appointments registered and supplied by the Social Care Institution to the research team with the authorization of the participants.

Secondary Outcome Measures

Full Information

First Posted
May 29, 2019
Last Updated
May 8, 2023
Sponsor
Iolanda Costa Galinha
Collaborators
DGArtes - Direção Geral das Artes, CIS-Iscte - Centro de Investigação e Intervenção Social
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1. Study Identification

Unique Protocol Identification Number
NCT03985917
Brief Title
Singing Groups for Seniors: Well-Being, Cognitive Function and Health
Acronym
Sing4Health
Official Title
"Grupos de Canto Para Seniores" Despacho Nº 11409-C/2017, Projeto n.º 626, From Orçamento Participativo Portugal, Ministério da Cultura
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
December 5, 2018 (Actual)
Primary Completion Date
February 20, 2019 (Actual)
Study Completion Date
February 28, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Iolanda Costa Galinha
Collaborators
DGArtes - Direção Geral das Artes, CIS-Iscte - Centro de Investigação e Intervenção Social

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Function, Well-Being, Physical Function, Respiratory Function, Memory, Biomarker, Anxiety, Depression, Stress, Quality of Life, Loneliness, Social Identification, Blood Pressure, Blood Glucose, Cholesterol, C-reactive Protein, Erythrocyte Sedimentation Rate, Balance, Sleep, Pain Perception, Medication Compliance, Health Complaint, Subjective, Body Weight
Keywords
Singing Group, Choir, Intervention, Older Adults, Well-Being, Cognitive Function, General Health

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants were recruited by invitation in the day-care centers, nursing homes and home care units run by Santa Casa da Misericórdia (a Portuguese Charity Institution, partner in the project). All older adults received an invitation with a brief description of the program and the study. In case they were interested in participating, they were invited to a meeting where the musical intervention team provided additional information about the intervention and clarified any questions from the participants. At the end of the session a detailed informed consent was signed.
Masking
Outcomes Assessor
Masking Description
Participants, singing group facilitators and researchers conducting the study cannot be blinded to allocation. However, the collection of the data, namely, cognitive, psychosocial, motor and physiologic outcome measures will be assessed by independent researchers, blinded to group allocation.
Allocation
Randomized
Enrollment
140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Singing Group Program
Arm Type
Experimental
Arm Description
Singing group intervention program that includes six components: (1) vocal warm-up exercises; (2) vocal technique; (3) rehearsal of repertoire; (4) break for socialization; (5) creation and presentation of a show; (6) assessment of participants performance (vocal tuning).
Arm Title
Alternative Social and Leisure Activities
Arm Type
Active Comparator
Arm Description
While the experimental group is participating in the intervention program, the control group will participate in the other activities proposed by the day care centers, which will be registered.
Intervention Type
Other
Intervention Name(s)
Singing Group Intervention Program
Other Intervention Name(s)
Choir Intervention Program
Intervention Description
Each session will start with (1) relaxation, vocal warm-up and breething exercises; (2) vocal technique training; (3) memorization and interpretation of music and lyrics; (4) session breaks of 20 minutes for socialization; (5) preparation of a final choir show; (6) vocal tuning tests.
Intervention Type
Other
Intervention Name(s)
Alternative Social and Leisure Activities
Other Intervention Name(s)
Social and Leisure Activities
Intervention Description
Day care centers provide social and leisure activities opportunities for older adults. The control group is free to enroll in these activities.
Primary Outcome Measure Information:
Title
Quality of Life - WHOQOL-BREF
Description
The WHOQOL-BREF measures the subjective perception of quality of life. It consists of 26 items, of which two items measure global quality of life and 24 items measure four dimensions. In this study the (1) Physical health, (2) Psychological Health, (3) Social relationships will be measured. The items are answered in a 5 point scale, from 1 (Very Bad; Very Unsatisfied; Nothing; Never) to 5 (Very Good; Very Satisfied; Extremely; Always).
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Quality of Life - WHOQOL-OLD
Description
The WHOQOL-OLD measures the quality of life specifically for older adults, with 28 items, measuring six dimensions. In this study the dimensions (1) sensory abilities; (2) autonomy; (3) past, present, and future activities; and (4) social participation will be measured. The items are answered in a 5-point scale, from 1 (Nothing; Very Bad; Very Unsatisfied) to 5 (Extremely; Very Good; Very Satisfied).
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Depression, Anxiety and Stress - Dass 21
Description
The DASS 21 measures Anxiety, Depression and Stress. Consists of 21 items distributed in 3 subscales of 7 items each, answered on a 4-point scale, ranging from: 0 "It did not apply to me", to 3 "Applied to me most of the time".
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Positive and Negative Affect - PANAS
Description
Measures the frequency of positive and negative emotions, during the past four months, and consists of two scales with 10 items each, answered on a 5-point scale from: 1 "nothing or very slightly"; to 5 "extremely".
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Life Satisfaction - SWLS
Description
Measures satisfaction with life in general, according to the persons' criteria. Consists of five items, answered on a 5-point scale from: 1 = strongly disagree; to 5 - I agree very much.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Self-Esteem - RSES
Description
Measures the appreciation of self-worth and self-acceptance, with 10 items, answered on a 4-point Likert scale, from: 1 = strongly disagree; to 4 = strongly agree.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Loneliness - UCLA Loneliness Scale
Description
Measures the feeling of being cut off from others, with four items, derived from the longer version of the ULS-20, answered on a 4-point scale from: 0 (Never), to 4 (Often / Many Times).
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Social Identification - FISI
Description
Measures the emotional evaluation of the relationship between the self and the ingroup, with four items, answered on a 7-point scale, ranging from: 1 "strongly disagree", to 7 "strongly agree".
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Social Well-Being - Scale of Social Well-Being
Description
Measures a multidimensional construct of social well-being including the dimensions: social acceptance, social coherence, social actualization, social integration and social contribution. Constituted by 33 items, answered on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree).
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Cognitive Function - MoCA
Description
Measures six cognitive functions: executive function; visuospatial skills; short-term memory; language; attention, concentration and working memory; and temporal and spatial orientation. The test is constituted by six groups of tasks and exercises. The maximum score is 30 points; higher scores indicate better cognitive performance.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Short-term auditory verbal memory - RAVELT
Description
The scale measures the rate of verbal learning, learning strategies, retroactive, and proactive interference, presence of confabulation or confusion in memory processes, retention of information, and differences between learning and retrieval. It consists of a list of 15 unrelated words repeated over five different trials, which participants are asked to repeat.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Attention and Executive Function - Trail Making Test
Description
The test measures the processing speed, mental flexibility, and divided attention. It consists of a task of connecting a trail of numbers with a drawing line. In this study, TMT A will be used, providing two direct scores: time to complete part A and performance errors.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Processing Speed - Digit Symbol Test
Description
The test measures the processing speed of non-verbal information. It consists of a task of drawing figures corresponding to numbers. It also measures cognitive and motor speed, planning ability, visual memory, visuomotor coordination, motivation to perform the task and attention.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Blood Pressure - Licensed laboratory
Description
Measures the pressure with which the blood circulates within the arteries. Data collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Pulse - Licensed laboratory
Description
The count of arterial pulse per minute, measures the number of times the heart beats per minute. Data collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Glycemia - Blood sample - Licensed laboratory
Description
Measures the amount of glucose present in the blood, used in the diagnosis and treatment of several diseases as diabetes mellitus or hypoglycemia. Data is collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Cholesterol - Blood sample - Licensed laboratory
Description
Measures total cholesterol, a fatty substance produced by the liver, present in all body cells and essential for the formation of the cell membranes hormone synthesis, digestion of fats, production of bile, metabolism of vitamins A, D, E and K, important in the constitution of global coronary disease risk. Data is collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
C-reactive protein (CRP) - Blood sample - Licensed laboratory
Description
Measures C-reactive protein, a protein produced in the liver and in case of inflammatory states its production increases. Indicates an ongoing, but not specific, organism infection. It can also be high in case of neoplasia. Data collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Erythrocyte Sedimentation Rate (ESR) - Blood sample - Licensed laboratory
Description
A measure of the red blood cells sedimentation by micro photometry over a period of time. A blood sedimentation rate is tested to detect inflammation in the body or to follow the progress of a disease. Data is collected and analyzed by a licensed laboratory.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Body Weight - Professional scale
Description
Body weight is assessed by weighing the person with light clothing, without shoes and while fasting.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Respiratory Function - Spirometry (Medikro Pro) - Air Volume
Description
The test consists of a simple examination, which allows to globally evaluate how the lungs are functioning by measuring the volume of air (measured in litres with the tests FVC, FEV1 and FEV6). In addition the Tiffeneau-Pinelli Index will be measured, which is a ratio between FVC and FEV1. Data is collected by trained researchers in motricity sciences.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Respiratory Function - Spirometry (Medikro Pro) - Air Speed
Description
The test consists of a simple examination, which allows to globally evaluate how the lungs are functioning by measuring the speed of air expired (litres per second, measured with the tests PEF, FEF 25 to 75%). Data is collected by trained researchers in motricity sciences.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Body Balance - Unipedal Stance Test.
Description
The participant is instructed to balance on a foot of their choosing for up to 20 seconds. The number of seconds in balance is registered as the score of this test. Data collected by trained researchers in motricity sciences.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Physical Activity - Actigraphy (GT3X accelerometer)
Description
Actigraphy registers the body accelerations in three axes (vertical, antero-posterior, and medio-lateral). Participants will be asked to wear the accelerometer around the hip for seven consecutive days (day and night, except when bathing). The accelerometer provides a measure of the frequency, intensity, and duration of physical activity and allows for the classification of activity levels as sedentary, light, moderate and vigorous.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Sleep Quality - Actigraphy (GT3X accelerometer)
Description
Actigraphy registers the body accelerations in three axes (vertical, antero-posterior, and medio-lateral). Participants will be asked to wear the accelerometer around the hip for seven consecutive days (day and night, except for bathing). The accelerometer provides a measure of the frequency, intensity, and duration of physical activity and allows for a measure of the total duration of sleep.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Pain Perception - The Brief Pain Inventory,
Description
The scale measures different types of pain, with nine questions: a first one that is optional; a second one based on drawings of the human body to locate the pain in the body; four items about pain intensity (worst pain, least pain, average pain, pain right now); two items on pain relief or medication; and one item on pain interference, with seven sub-items (general activity, mood, walking ability, normal walk, relations with other people, sleep, and enjoyment of life). Answering options from: 0 "No pain / Did not interfered"; and 10 "The greatest pain possible / Completely interfered".
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Medication Intake - Social Support Institution
Description
Medication and dosage are registered and supplied by the Social Care Institution to the research team with the authorization of the participants.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).
Title
Health Services Attendance - Social Support Institution
Description
Number and type of health services appointments registered and supplied by the Social Care Institution to the research team with the authorization of the participants.
Time Frame
Change from baseline at 4 months (post-test) and at 10 months (follow-up).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion criteria: Being 60 years old or older; Retired; Accept the invitation to participate in the singing group program; Not having participated in other intervention programs in the previous four months. Exclusion criteria: Having a severe impairment, that is disabling for the participation in the singing group activity (e.g. severe cognitive, auditory, visual or mobility impairments).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iolanda C. Galinha, Ph.D,
Organizational Affiliation
Universidade Autónoma de Lisboa
Official's Role
Study Director
Facility Information:
Facility Name
Universidade Autónoma de Lisboa
City
Lisbon
ZIP/Postal Code
1150-293
Country
Portugal

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34378330
Citation
Galinha IC, Garcia-Martin MA, Lima ML. Sing4Health: Randomised controlled trial of the effects of a singing group program on the subjective and social well-being of older adults. Appl Psychol Health Well Being. 2022 Feb;14(1):176-195. doi: 10.1111/aphw.12297. Epub 2021 Aug 10.
Results Reference
derived
PubMed Identifier
32948120
Citation
Galinha IC, Farinha M, Lima ML, Palmeira AL. Sing4Health: protocol of a randomized controlled trial of the effects of a singing group intervention on the well-being, cognitive function and health of older adults. BMC Geriatr. 2020 Sep 18;20(1):354. doi: 10.1186/s12877-020-01686-6.
Results Reference
derived
Links:
URL
https://dre.pt/home/-/dre/114422404/details/maximized
Description
Projeto n.º 626, from Orçamento Participativo Portugal, Ministério da Cultura

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Singing Groups for Seniors: Well-Being, Cognitive Function and Health

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