Adaptive Music Therapy for Psychosocial and Cognitive Functions of Older Adults
NCT05447312, Not applicable, Active not recruiting, Toronto Metropolitan University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Adaptive Music Therapy for Psychosocial and Cognitive Functions of Older Adults | ClinicalTrials.gov |
| NCT number | NCT05447312 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 75 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Toronto Metropolitan University | ClinicalTrials.gov |
| Conditions | Stress, Psychological, Executive Functions, Loneliness, Emotion Regulation, Functional Abilities, Well Being | ClinicalTrials.gov |
| Interventions | Adaptive Music Intervention, Traditional Music Intervention | ClinicalTrials.gov |
| First posted | 2022-07-07 | ClinicalTrials.gov |
| Last updated | 2026-09-04 | ClinicalTrials.gov |
Registered outcomes 7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Quality of life: Psychosocial functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on Qualtrics, no cut off scores. Psychosocial functioning will be assessed using the: -World Health Organization - 5. Higher scores indicate increased quality of life. | ClinicalTrials.gov |
| Primary | Resiliency: Psychosocial functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on Qualtrics, no cut off scores. Psychosocial functioning will be assessed using the: -Brief Resilient Coping Scale. Higher scores indicates higher resiliency coping. | ClinicalTrials.gov |
| Primary | Emotional Regulation: Psychosocial functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on Qualtrics, no cut off scores. Psychosocial functioning will be assessed using the: -Emotion Regulation Questionnaire. Higher scores indicate increased emotional regulation. | ClinicalTrials.gov |
| Primary | Activities of Daily Living: Psychosocial functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on Qualtrics, no cut off scores. Psychosocial functioning will be assessed using the: -Lawton Instrumental Activities of Daily Living Scale. Higher scores indicate better everyday functioning. | ClinicalTrials.gov |
| Primary | Loneliness: Psychosocial functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on Qualtrics, no cut off scores. Psychosocial functioning will be assessed using the: \- 6-item de Jong Gierveld. Higher scores indicate increased loneliness. | ClinicalTrials.gov |
| Primary | Emotional processing: Cognitive functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on PsychoPy. Cognitive performance will be measured using the: -Emotional Stroop Task. Increased reaction time to negative emotional words indicates decreased mood. | ClinicalTrials.gov |
| Primary | Processing Speed: Cognitive functions of healthy older adults. | Baseline (pretest), 4 weeks (posttest), and 16 weeks (3-month follow-up), | All computerized on PsychoPy. Cognitive performance will be measured using the: -Digit Symbol Substitution Test. Increased accuracy indicates better processing speed efficiency. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 20
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 1202204 | BACKGROUND | PubMed |
| 3397865 | BACKGROUND | PubMed |
| 5349366 | BACKGROUND | PubMed |
| 8711015 | BACKGROUND | PubMed |
| 10916193 | BACKGROUND | PubMed |
| 12916575 | BACKGROUND | PubMed |
| 14994958 | BACKGROUND | PubMed |
| 15842075 | BACKGROUND | PubMed |
| 23362501 | BACKGROUND | PubMed |
| 24009169 | BACKGROUND | PubMed |
| 24933485 | BACKGROUND | PubMed |
| 26029120 | BACKGROUND | PubMed |
| 27094452 | BACKGROUND | PubMed |
| 27405091 | BACKGROUND | PubMed |
| 28149509 | BACKGROUND | PubMed |
| 28290068 | BACKGROUND | PubMed |
| 30124583 | BACKGROUND | PubMed |
| 34602963 | BACKGROUND | PubMed |
| 35206924 | BACKGROUND | PubMed |
| 35263341 | BACKGROUND | PubMed |
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Emotional Stroop Task | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Symbol Coding | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)