Trial · NCT04515758
Determining the Feasibility of Implementing a Combined Cognitive and Exercise Training Program for Older Adults in a Community Setting.
NCT04515758, Not applicable, Completed, University of Waterloo
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Determining the Feasibility of Implementing a Combined Cognitive and Exercise Training Program for Older Adults in a Community Setting. Trials, record NCT04515758. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04515758
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Determining the Feasibility of Implementing a Combined Cognitive and Exercise Training Program for Older Adults in a Community Setting.
- NCT number
- NCT04515758
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 43 participants, actual
- Lead sponsor
- University of Waterloo
- Conditions
- Osteo Arthritis, Osteoporosis, Joint Replacement, Fibromyalgia, High Blood Pressure, Stable Heart Conditions, Chronic Obstructive Pulmonary Disease, Diabetes, Obesity
- Interventions
- Exercise and Cognitive Training, Exercise Training Only
- First posted
- 2020-08-17
- Last updated
- 2020-08-17
Source ClinicalTrials.gov
Registered outcomes30
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Recruitment Rate | Pre-program (baseline) | Total number of people enrolled divided by the total number of people invited to participate (multiplied by 100 to calculate a percentage) |
| Primary | Completion Rate | Through study completion, 12 weeks | Percentage of people who completed the full program and all assessments |
| Primary | Attendance | Throughout entire intervention (12 weeks, 2 sessions/week per group) | Percentage of people who attended program sessions (exercise and cognitive training components) |
| Primary | Change in Participant and Instructor Rating of experience, satisfaction, and feasibility of program | Mid-point (6 weeks) and post-program (12 weeks) | Participant and instructors rating of program components and overall program (via hand-written questionnaire). Participants and instructors must rate their level of agreement (1 = strongly disagree, 2 = disagree, 3 = no opinion, 4 = agree, 5 = strongly agree) with various statements. The higher the rating, the greater the satisfaction. They also must rate if the difficulty of the program was optimal, somewhat easy or hard, or too easy or hard. They must also specify how much money they would be willing to spend on the program. They are also given an opportunity to record optional additional comments/recommendation. |
| Primary | Cost of program | Post-program (12 weeks) | Financial cost of running program (equipment purchased for study - cognitive training tablet and stands - and YMCA staff pay) as reported by researcher and YMCA staff |
| Primary | Sex | Pre-program (baseline) | Self-reported biological sex (at birth) using basic demographics questionnaire |
| Primary | Participant and Instructor perceived program experience and satisfaction | Post-program (at 12 weeks) | One-on-one interview with researcher, answering broad questions about their experience in the program and study |
| Primary | Participant and Instructor observer-perceived program experience and satisfaction | Throughout entire intervention (12 weeks, 2 sessions/week per group) | Experience of participants and instructors will also be observed by the researcher (observational notes will be taken by the researcher during each class). No names of participants and instructors will be recorded. |
| Primary | Education | Pre-program (baseline) | Self-reported years of formal education and training (training years for instructors only) using basic demographics questionnaire |
| Primary | Occupation | Pre-program (baseline) | Self-reported previous and current occupations using basic demographics questionnaire |
1 to 10 of 30Source ClinicalTrials.gov
See all 30 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
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 |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
| Task Switching Test | Secondary outcome | ConductCognition |
| Trail Making Test A | Secondary outcome | ConductCognition |
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04515758
GET https://conductscience.org/api/trials/v1/NCT04515758/registered?page=2