Trial · NCT05266911
Home-based HIFST for Older Adults to Prevent Functional Decline
NCT05266911, Not applicable, Completed, McMaster University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Home-based HIFST for Older Adults to Prevent Functional Decline. Trials, record NCT05266911. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05266911
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Home-based HIFST for Older Adults to Prevent Functional Decline
- NCT number
- NCT05266911
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 24 participants, actual
- Lead sponsor
- McMaster University
- Conditions
- Mobility Limitation, Fall Injury, Slip and Fall
- Interventions
- high-intensity functional strength training, Lower extremity stretching
- First posted
- 2022-03-04
- Last updated
- 2023-09-21
Source ClinicalTrials.gov
Registered outcomes17
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Feasibility: Adherence | over 12 weeks (intervention duration) | Percentage of exercise sessions completed (criteria: at least 70 precent) |
| Primary | Feasibility: Recruitment | 4-6 month recruitment period | Percentage of eligible participants recruited (criteria: at least 65 precent) |
| Primary | Feasibility: Retention | over 12 weeks | Percentage of participants completing baseline and follow-up assessments (criteria: at least 80 percent) |
| Primary | Feasibility: Safety (number/presence of intervention-related serious adverse events) | over 12 weeks (intervention period) | Adverse events related to intervention (criteria: no serious events) |
| Secondary | Physical Functioning: 4 meter walk test ( | pre and post intervention (12 weeks) | usual gait speed over 4 meters |
| Secondary | Physical Functioning: dual-task cognitive Timed Up and Go (TUG-COG) | pre and post intervention (12 weeks) | time to rise from a standard chair, walk 3 meters, turn around, walk back to the chair and sit down while counting backwards by three |
| Secondary | Physical Functioning: Two minute step test (TMST) | pre and post intervention (12 weeks) | number of steps in two minutes |
| Secondary | Physical Functioning: 30-second chair stand test (30CST) | pre and post intervention (12 weeks) | number of full stands from a chair in 30 seconds |
| Secondary | Physical Functioning: Preclinical Mobility Limitation (PCML) scale | pre and post intervention (12 weeks) | classified as no mobility limitation, preclinical mobility limitation, minor manifest limitation or major manifest limitation for 3 tasks (walking 0.5km, walking 2 km, and climbing one flight of stairs) |
| Secondary | Cognitive Functioning: California Older Adult Stroop Test (COAST) | pre and post intervention (12 weeks) | measures executive functioning by assessing the ability to inhibit an automatic response |
1 to 10 of 17Source ClinicalTrials.gov
See all 17 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.
Tests4
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 |
| Symbol Coding | Secondary outcome | ConductCognition |
| Trail Making Test A | Secondary outcome | ConductCognition |
| Trail Making Test B | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT05266911
GET https://conductscience.org/api/trials/v1/NCT05266911/registered