Trial · NCT07897929
Exercise and Fall Prevention for Fracture Reduction
NCT07897929, Not applicable, Not yet recruiting, Wolfgang Kemmler, PhD
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Exercise and Fall Prevention for Fracture Reduction. Trials, record NCT07897929. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07897929
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Exercise and Fall Prevention for Fracture Reduction
- NCT number
- NCT07897929
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 72 participants, estimated
- Lead sponsor
- Wolfgang Kemmler, PhD
- Conditions
- Osteopenia, Osteoporosis, High Fall Risk
- Interventions
- Guideline-based home exercise training
- First posted
- 2026-10-27
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Changes of chair rise test performance | Changes in the 5tStS from the baseline measurement to the 16-week follow-up (FU) assesment | Time for the 5 times sit to stand test (5tSTS) in s |
| Primary | Changes in static balance performance | Changes in balance performance from the baseline measurement to the 16-week follow-up (FU) assessment. | Balance performance applying the modified balance test based on the Short Physical Performance Battery (SPPB). Score from 0-4 with higher values indicationg better static balance |
| Secondary | Changes in the timed up and go test (TUG) | Changes in the TUG test results from the baseline measurement to the 16-week follow-up. | TUG: Time needed to stand up, walk 3 meters, turn, return, and sit down (in s) |
| Secondary | Changes in habitual walking speed | Changes in the habitual walking speed from the baseline measurement to the 16-week follow-up. | Habitual walking speed over 10 metres, measured using photoelectric sensors (in s) |
| Secondary | Changes in maximum strength of the hip- and leg-extensors | Changes in the isokinetic maximum strength of the hip- and leg-extensors from the baseline measurement to the 16-week follow-up. | Isokinetic maximum strength of the hip- and leg-extensors as determined by an isokinetic leg press (NM) |
| Secondary | Change in maximum trunk extensors strength | Change in the maximum isometric strength of the trunk extensors from the baseline measurement to the 16-week follow-up. | Maximum isometric strength of the trunk extensors (kg) as determined by a Dr. Wolff BackCheck |
| Secondary | Changes in fear of falling | Change in FES I from the baseline measurement to the 16-week follow-up. | Fear of falling as determined by the "Short Falls Efficacy Scale-International" (FES I). 7 Items, Score from 7-28, with higher scores indicating higher concerns of falling |
| Secondary | Changes in bone formation biomarkers | Change in PINP from the baseline measurement to the 16-week follow-up. | Changes in the bone formation marker "Procollagen Type I N-terminal Propeptide" (PINP, ng/ml)) as determined by Enzyme-Linked Immunosorbent Assay (ELISA). Note: Only in women not receiving medication for osteoporosis |
| Secondary | Changes in bone resorption biomarkers | Change in CTX from the baseline measurement to the 16-week follow-up. | Changes in the bone resorption marker "C-terminal telopeptide of type I collagen" (CTX, ng/ml) as determined by Enzyme-Linked Immunosorbent Assay (ELISA). Note: Only in women not receiving medication for osteoporosis |
| Secondary | Changes in fat free mass | Change in FFM from the baseline measurement to the 16-week follow-up. | Fat free mass (FFM, kg, g) as determined by Bioelectrical Impedance Analysis (BIA) |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 41699562 | BACKGROUND |
Source PubMed
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.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
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/NCT07897929
GET https://conductscience.org/api/trials/v1/NCT07897929/registered