Fall PreventionPRE'PASNCT07758764
The Balance and Foot Health Program for Older Adults: A Randomized Study
A study testing Weekly foot health workshops and Balance Workshops in people with Fall Prevention, run by Centre Hospitalier Emile Roux at 20 sites in France.
Trial summary
Every year in France, 2 million falls by people over 65 are responsible for 10,000 deaths, the leading cause of accidental death, and more than 130,000 hospitalizations. The primary objective of this study is to compare the effectiveness of adding 12 weekly foot health workshops to balance workshops on mobility among… Read more about this study
- Who is it for?
- Ages 65 years and older
- Conditions the study is for
- Fall Prevention
- What is being tested?
- Weekly foot health workshops and Balance Workshops
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 20 sitesFrance
- Study dates
- 20 Aug 2026to 1 Jul 2029
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 years and older
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- People aged 65 and older.
- Residents of nursing homes.
- Able to walk, with or without a walking aid (cane, walker, etc.)
- Residents at risk of falling, defined by at least one of the following criteria: history of a fall within the last 12 months; unsteadiness while walking or balance issues; limited mobility.
- Able to understand and follow simple instructions.
- Able to participate in workshops.
- Enrolled in a social security program or beneficiaries of an equivalent program.
- Individuals (participants, guardians, or conservators, as applicable) who have been informed and have provided written consent for their participation in the study.
Who cannot join
- Regular use of minimalist shoes at the time of enrollment.
- Medical condition or clinical situation contraindicating the use of minimalist shoes, as determined by the investigator.
- Use of orthopedic shoes prescribed by a healthcare professional.
- Unhealed foot wound or active foot infection.
- Recent lower limb fracture (< 3 months) or recent lower limb trauma, likely to limit participation in the workshops or contraindicate foot mobilization, as assessed by the investigator.
- Severe cognitive impairment preventing the understanding of simple instructions or participation in the workshops.
- Any other clinical condition deemed incompatible with participation in the study by the investigator.
Trial locations and contacts
20 sites in 1 country. Contact the study team or a site near you to ask about taking part.
20 sites in 1 country
France20 sites, 20 recruiting
- Recruiting
EHPAD " Les 2 Volcans"
Allègre, 43270
Herve Fundenberger, PhD, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Foyer Notre-Dame"
Beaulieu, 43800
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Bon secours"
Beauzac, 43590
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Vert Bocage"
Brives-Charensac, 43700
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Sainte Monique"
Coubon, 43700
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Recruiting
EHPAD "Saint Dominique"
Craponne-sur-Arzon, 43500
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Recruiting
EHPAD Centre Hospitalier du Pays De Craponne
Craponne-sur-Arzon, 43500
Hervé Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Le grand pré "
Lantriac, 43260
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Les Terrasses de la Gazeille"
Le Monastier-sur-Gazeille, 43150
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Bel Horizon"
Le Puy-en-Velay, 43000
Hervé Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Les Patios du Velay"
Le Puy-en-Velay, 43000
Herve Fundenberger, PhD, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "L'Age d'Or"
Monistrol-sur-Loire, 43120
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Résidence des Bords de Loire"
Retournac, 43130
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Résidence La Roseraie"
Rosières, 43800
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "la Tortue"
Saint-Julien-Chapteuil, 43260
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "l'Orangeraie"
Saint-Maurice-de-Lignon, 43200
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Recruiting
EHPAD "Résidence Ruessium"
Saint-Paulien, 43350
Herve Fundenberger, PhD, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Résidence Sainte Sigolène"
Sainte-Sigolène, 43600
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Foyer Bon Accueil"
Solignac-sur-Loire, 43370
Hervé Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
- Not yet recruiting
EHPAD "Foyer Marie Goy"
Vorey, 43800
Herve Fundenberger, 04 71 04 35 38, hervefundenberger@ch-lepuy.fr
About this study
Every year in France, 2 million falls by people over 65 are responsible for 10,000 deaths, the leading cause of accidental death, and more than 130,000 hospitalizations. The primary objective of this study is to compare the effectiveness of adding 12 weekly foot health workshops to balance workshops on mobility among older adults living in nursing homes, compared to a program based exclusively on balance workshops.
Read the detailed description
The purpose of this multicenter cluster-randomized controlled trial is to evaluate whether a structured Foot Health Program combined with balance training improves functional outcomes in nursing home residents compared with balance training alone.
Foot disorders are common among older adults living in nursing homes and may contribute to impaired balance, reduced mobility, loss of functional independence, and increased risk of falls. Interventions targeting foot health, sensory stimulation, foot mobility, and foot muscle strengthening may represent an innovative approach to complement conventional fall prevention strategies. This study aims to assess the added value of a multimodal foot-focused intervention when combined with a standardized balance training program.
Twenty nursing homes (EHPADs) will participate in the study. Nursing homes will be randomized at the facility level in a 1:1 ratio to either the intervention group or the control group. Ten facilities will be allocated to the intervention group and ten facilities to the control group. A total of 200 participants will be enrolled, with approximately 10 residents recruited in each nursing home.
Prior to enrollment, eligibility criteria will be assessed during a screening visit. Study information will be provided to participants and, when applicable, to their legal representative or trusted person. Written informed consent will be obtained before participation in any study procedures.
At baseline (T0), demographic and clinical characteristics will be collected. All participants will undergo a podiatric assessment performed by a podiatrist involved in the study. Routine foot care will be provided when required. Baseline outcome assessments will be completed within 15 days before the first intervention session.
Participants allocated to the intervention group will receive a structured Foot Health Program in addition to standardized balance workshops. The Foot Health Program consists of 12 weekly sessions delivered by a mobile nurse trained in foot massage techniques and foot health education. The intervention was developed and refined through a feasibility study and subsequently standardized to ensure reproducibility across participating nursing homes.
The Foot Health Program is organized into three sequential phases. The first phase (sessions 1 to 3) focuses on foot preparation. Participants attend individual weekly sessions lasting approximately 30 minutes. Sessions include foot massage, sensory stimulation activities, and gentle foot mobilization exercises. Participants are encouraged to perform selected exercises independently between sessions. Minimalist footwear is introduced at the end of this phase and may be used outside supervised sessions according to participant preference and tolerance.
The second phase (sessions 4 to 6) focuses on transition toward active exercise. Participants attend weekly group sessions lasting approximately 45 minutes. Activities emphasize foot and ankle mobility, strengthening of intrinsic and extrinsic foot muscles, and progressive motor control exercises. Brief foot massage is maintained as preparation for exercise.
The third phase (sessions 7 to 12) focuses on stabilization and functional integration. Participants continue weekly group sessions and progressively incorporate minimalist footwear into the intervention. Exercises acquired during previous phases are reinforced and integrated into functional activities involving posture, balance, gait, and mobility. The objective is to facilitate transfer of acquired abilities into daily activities and support functional autonomy.
Participants allocated to the control group will receive balance workshops only.
All participants, regardless of group allocation, will participate in a standardized balance training program. Balance workshops will be conducted once weekly for approximately one hour throughout the study period. Sessions may be delivered by external adapted physical activity providers, adapted physical activity professionals employed by the facility, or physiotherapists, depending on local organization. To ensure consistency across study sites, all instructors will follow a predefined exercise framework and standardized session structure. Sessions will include warm-up exercises, static and dynamic balance training, and functional strengthening activities. Exercise intensity and difficulty may be adapted to individual participant abilities while preserving the core components of the program.
Following completion of the initial 12-week intervention period, participants in both groups will continue attending weekly balance workshops for an additional 12 weeks. During this follow-up period, no Foot Health Program sessions will be provided.
Outcome assessments will be performed at three time points. Baseline assessments (T0) will be conducted within 15 days before the first intervention session. Post-intervention assessments (T1) will be conducted within 15 days after completion of the first 12 sessions. Follow-up assessments (T2) will be conducted after completion of the additional 12 weeks of balance training.
In addition to study outcome measures, data collected at T1 will include attendance rates, adherence to the intervention, participant satisfaction with the workshops, satisfaction with minimalist footwear, and footwear utilization. At T2, satisfaction with footwear and continued footwear use will be reassessed.
All study data collected at T0, T1, and T2 will be recorded by trained members of the study team and entered into an electronic case report form (eCRF) by qualified clinical research personnel.
The study is designed to determine whether a multimodal intervention targeting foot health provides additional benefits beyond standardized balance training alone in nursing home residents and may contribute to the development of new strategies for maintaining mobility, balance, and functional independence in this population.
- Conditions
- Fall Prevention
- Being tested
- Weekly foot health workshops, Balance Workshops
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Weekly foot health workshopsOther
Combination of minimalist footwear, foot massages, and workshops to re-learn walking and posture, 12 workshops are planned, every week.
Balance WorkshopsOther
Participants will take part in 12 balance workshops following a standardized format, including warm-up exercises, static and dynamic balance exercises, and functional strength training.
| Study group | Role | What they receive |
|---|---|---|
| Experimental Group | Experimental | Participants in the intervention group will attend weekly workshops as part of the Foot Health program (12 sessions), led by a mobile nurse trained in massage. The mobile nurse will perform all massages and lead the foot health workshops for all participants in the intervention group. Her status as a healthcare professional ensures the safety of the intervention. In addition, she is trained in wellness massage techniques.
Participants will also take part in 12 workshops focused on balance, led by a professional in adapted physical activity. This workshop will include recommended strength training and balance exercises. Receives: Other: Weekly foot health workshops; Other: Balance Workshops |
| Control group | Active comparator | The control group will participate only in 24 balance workshops. Balance workshops have been developed over the past decade to improve the independence of nursing home residents. However, their implementation varies widely from one facility to another, with differences in content, frequency, and instructors. This variability underscores the need to establish a common framework to ensure the comparability of interventions in a research setting. Receives: Other: Balance Workshops |
What is being measured
The primary outcome is the main question the study is designed to answer.
The change in the Timed Up and Go test time, expressed in seconds
The Timed Up and Go is a commonly used screening tool to assess mobility in older adults. The participant must stand up from a chair, walk a distance of three meters, turn around, then walk back to the chair and sit down. These tasks must be performed in a comfortable and safe pace. A practice trial is allowed to help the individual become familiar with the task. The individual wears their usual shoes. The use of a walking aid is permitted, but its use must be noted on the data collection form. No physical assistance is provided. The TUG is also sensitive to changes, detecting improvements or deteriorations in functional mobility. It has high validity, being able to correctly identify fallers and non-fallers with a sensitivity and specificity of 87%. Finally, this test is accurate, simple to administer, and useful for assessing functional mobility, particularly in older or medically compromised populations.
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1)
Secondary outcomes (9)
Changes in the position of the center of pressure during static stance
Changes in the movement of the center of pressure in a static position, measured using a stabilometry platform, with eyes open and closed, at baseline assessment (T0), after the foot care intervention (T1), and at the end of the study (T2).
Postural control is generally assessed by analyzing the length of the center of pressure trajectory, which quantifies the extent of body sway and stability while standing. The displacement of the center of pressure is widely recognized as one of the most reliable indicators of postural stability 43. When the eyes are open, postural control relies primarily on the visual system, whereas when the eyes are closed, the vestibular system, proprioceptive inputs, and plantar mechanoreceptors play a more significant role in maintaining balance.
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in the muscle strength of the flexors of the big toes (hallux)
Changes in muscle strength of the big toe flexors (hallux) measured using a dynamometer (The Toe Strength Dynamometer) at baseline assessment (T0) and after the foot care intervention (T1) and the end of the study (T2).
In older adults, muscle strength loss has recently emerged as a risk factor for falls. The dynamometer used in this study demonstrated moderate to excellent intra-rater reliability, as well as good to excellent inter-rater reliability for all measurements.
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in ankle joint range of motion during dorsiflexion and plantar flexion
Changes in ankle joint range of motion in dorsiflexion and plantar flexion, measured using a digital goniometer, at baseline assessment (T0) and after the foot care intervention (T1) and the end of the study (T2).
The Weight-Bearing Lunge test is commonly used to assess the range of dorsiflexion of the ankle. However, during our feasibility study, it proved difficult to perform in a population of very elderly individuals. To overcome this difficulty, we will use a digital goniometer.
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in participants' fear of falling
Changes in participants' fear of falling, measured using a 0-10 numerical rating scale at baseline assessment (T0) and after the foot care intervention (T1) and the end of the study (T2).
The use of a binary question to assess fear of falling is reliable and easy to use in research and clinical practice, particularly in nursing homes.
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in foot pain experienced while walking
Changes in foot pain experienced while walking, measured at baseline assessment (T0) and after the foot care intervention (T1) and the end of the study (T2) using a numerical scale from 0 to 10;
Measured: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
The Evolution of Mobility Through the TUG
Changes in mobility as measured by the TUG, assessed after the foot care intervention (T1) and the end of the study (T2).
Measured: after the 12 intervention sessions (T1) and 6 months (T2).
The incidence of falls measured over the course of the study
The recording of falls during the study period, using fall reports from medical records and a patient questionnaire
Measured: From baseline assessment (T0) until 6 months (T2)
Participants' satisfaction with minimalist shoes and the various workshops
Participants' satisfaction with minimalist shoes and the various workshops, as measured by a questionnaire administered after the foot care intervention (T1) and the end of the study (T2).
Measured: after the 12 intervention sessions (T1) and 6 months (T2).
The number of hours per day that shoes were worn by participants in the experimental group
The number of hours per day that shoes were worn by participants in the experimental group following the foot care intervention (T1) and at the end of the study (T2), as reported via a questionnaire.
Measured: after the 12 intervention sessions (T1) and 6 months (T2).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Aug 2026
- Study start20 Aug 2026
- Primary completion1 Jan 2028 (estimated)
- Study completion1 Jul 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fall PreventionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Emile Roux
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07758764
- Sponsor's protocol ID
- RIPH2_FUNDENBERGER_PREPAS
- Other IDs
- 2026-A01073-48
- Acronym
- PRE'PAS
- Status last verified
- Nov 2026
- First submitted
- 3 Aug 2026
- Last updated
- 4 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Balance and Foot Health Program for Older Adults: A Randomized Study
- ClinicalTrials.gov ID
- NCT07758764
- Acronym / sponsor ID
- PRE'PAS / RIPH2_FUNDENBERGER_PREPAS
- Conditions
- Fall Prevention
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Centre Hospitalier Emile RouxUniversity, hospital or other
- Study start
- 20 Aug 2026 (actual)
- Primary completion
- 1 Jan 2028 (estimated)
- Study completion
- 1 Jul 2029 (estimated)
- First posted
- 11 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Every year in France, 2 million falls by people over 65 are responsible for 10,000 deaths, the leading cause of accidental death, and more than 130,000 hospitalizations. The primary objective of this study is to compare the effectiveness of adding 12 weekly foot health workshops to balance workshops on mobility among older adults living in nursing homes, compared to a program based exclusively on balance workshops.
Detailed description
The purpose of this multicenter cluster-randomized controlled trial is to evaluate whether a structured Foot Health Program combined with balance training improves functional outcomes in nursing home residents compared with balance training alone.
Foot disorders are common among older adults living in nursing homes and may contribute to impaired balance, reduced mobility, loss of functional independence, and increased risk of falls. Interventions targeting foot health, sensory stimulation, foot mobility, and foot muscle strengthening may represent an innovative approach to complement conventional fall prevention strategies. This study aims to assess the added value of a multimodal foot-focused intervention when combined with a standardized balance training program.
Twenty nursing homes (EHPADs) will participate in the study. Nursing homes will be randomized at the facility level in a 1:1 ratio to either the intervention group or the control group. Ten facilities will be allocated to the intervention group and ten facilities to the control group. A total of 200 participants will be enrolled, with approximately 10 residents recruited in each nursing home.
Prior to enrollment, eligibility criteria will be assessed during a screening visit. Study information will be provided to participants and, when applicable, to their legal representative or trusted person. Written informed consent will be obtained before participation in any study procedures.
At baseline (T0), demographic and clinical characteristics will be collected. All participants will undergo a podiatric assessment performed by a podiatrist involved in the study. Routine foot care will be provided when required. Baseline outcome assessments will be completed within 15 days before the first intervention session.
Participants allocated to the intervention group will receive a structured Foot Health Program in addition to standardized balance workshops. The Foot Health Program consists of 12 weekly sessions delivered by a mobile nurse trained in foot massage techniques and foot health education. The intervention was developed and refined through a feasibility study and subsequently standardized to ensure reproducibility across participating nursing homes.
The Foot Health Program is organized into three sequential phases. The first phase (sessions 1 to 3) focuses on foot preparation. Participants attend individual weekly sessions lasting approximately 30 minutes. Sessions include foot massage, sensory stimulation activities, and gentle foot mobilization exercises. Participants are encouraged to perform selected exercises independently between sessions. Minimalist footwear is introduced at the end of this phase and may be used outside supervised sessions according to participant preference and tolerance.
The second phase (sessions 4 to 6) focuses on transition toward active exercise. Participants attend weekly group sessions lasting approximately 45 minutes. Activities emphasize foot and ankle mobility, strengthening of intrinsic and extrinsic foot muscles, and progressive motor control exercises. Brief foot massage is maintained as preparation for exercise.
The third phase (sessions 7 to 12) focuses on stabilization and functional integration. Participants continue weekly group sessions and progressively incorporate minimalist footwear into the intervention. Exercises acquired during previous phases are reinforced and integrated into functional activities involving posture, balance, gait, and mobility. The objective is to facilitate transfer of acquired abilities into daily activities and support functional autonomy.
Participants allocated to the control group will receive balance workshops only.
All participants, regardless of group allocation, will participate in a standardized balance training program. Balance workshops will be conducted once weekly for approximately one hour throughout the study period. Sessions may be delivered by external adapted physical activity providers, adapted physical activity professionals employed by the facility, or physiotherapists, depending on local organization. To ensure consistency across study sites, all instructors will follow a predefined exercise framework and standardized session structure. Sessions will include warm-up exercises, static and dynamic balance training, and functional strengthening activities. Exercise intensity and difficulty may be adapted to individual participant abilities while preserving the core components of the program.
Following completion of the initial 12-week intervention period, participants in both groups will continue attending weekly balance workshops for an additional 12 weeks. During this follow-up period, no Foot Health Program sessions will be provided.
Outcome assessments will be performed at three time points. Baseline assessments (T0) will be conducted within 15 days before the first intervention session. Post-intervention assessments (T1) will be conducted within 15 days after completion of the first 12 sessions. Follow-up assessments (T2) will be conducted after completion of the additional 12 weeks of balance training.
In addition to study outcome measures, data collected at T1 will include attendance rates, adherence to the intervention, participant satisfaction with the workshops, satisfaction with minimalist footwear, and footwear utilization. At T2, satisfaction with footwear and continued footwear use will be reassessed.
All study data collected at T0, T1, and T2 will be recorded by trained members of the study team and entered into an electronic case report form (eCRF) by qualified clinical research personnel.
The study is designed to determine whether a multimodal intervention targeting foot health provides additional benefits beyond standardized balance training alone in nursing home residents and may contribute to the development of new strategies for maintaining mobility, balance, and functional independence in this population.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental Group | Experimental | Other: Weekly foot health workshops, Other: Balance WorkshopsParticipants in the intervention group will attend weekly workshops as part of the Foot Health program (12 sessions), led by a mobile nurse trained in massage. The mobile nurse will perform all massages and lead the foot health workshops for all participants in the intervention group. Her status as a healthcare professional ensures the safety of the intervention. In addition, she is trained in wellness massage techniques. Participants will also take part in 12 workshops focused on balance, led by a professional in adapted physical activity. This workshop will include recommended strength training and balance exercises. |
| Control group | Active comparator | Other: Balance WorkshopsThe control group will participate only in 24 balance workshops. Balance workshops have been developed over the past decade to improve the independence of nursing home residents. However, their implementation varies widely from one facility to another, with differences in content, frequency, and instructors. This variability underscores the need to establish a common framework to ensure the comparability of interventions in a research setting. |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
Key inclusion criteria (8 listed)
- People aged 65 and older.
- Residents of nursing homes.
- Able to walk, with or without a walking aid (cane, walker, etc.)
- Residents at risk of falling, defined by at least one of the following criteria: history of a fall within the last 12 months; unsteadiness while walking or balance issues; limited mobility.
- Able to understand and follow simple instructions.
Key exclusion criteria (7 listed)
- Regular use of minimalist shoes at the time of enrollment.
- Medical condition or clinical situation contraindicating the use of minimalist shoes, as determined by the investigator.
- Use of orthopedic shoes prescribed by a healthcare professional.
- Unhealed foot wound or active foot infection.
- Recent lower limb fracture (< 3 months) or recent lower limb trauma, likely to limit participation in the workshops or contraindicate foot mobilization, as assessed by the investigator.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Weekly foot health workshopsCombination of minimalist footwear, foot massages, and workshops to re-learn walking and posture, 12 workshops are planned, every week. | Other | Experimental Group |
| Balance WorkshopsParticipants will take part in 12 balance workshops following a standardized format, including warm-up exercises, static and dynamic balance exercises, and functional strength training. | Other | Control group, Experimental Group |
Primary outcome
The change in the Timed Up and Go test time, expressed in seconds
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1)
The Timed Up and Go is a commonly used screening tool to assess mobility in older adults. The participant must stand up from a chair, walk a distance of three meters, turn around, then walk back to the chair and sit down. These tasks must be performed in a comfortable and safe pace. A practice trial is allowed to help the individual become familiar with the task. The individual wears their usual shoes. The use of a walking aid is permitted, but its use must be noted on the data collection form. No physical assistance is provided. The TUG is also sensitive to changes, detecting improvements or deteriorations in functional mobility. It has high validity, being able to correctly identify fallers and non-fallers with a sensitivity and specificity of 87%. Finally, this test is accurate, simple to administer, and useful for assessing functional mobility, particularly in older or medically compromised populations.
9 secondary outcomes
Changes in the position of the center of pressure during static stance
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in the muscle strength of the flexors of the big toes (hallux)
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in ankle joint range of motion during dorsiflexion and plantar flexion
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in participants' fear of falling
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
Changes in foot pain experienced while walking
Time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1) and 6 months (T2).
The Evolution of Mobility Through the TUG
Time frame: after the 12 intervention sessions (T1) and 6 months (T2).
The incidence of falls measured over the course of the study
Time frame: From baseline assessment (T0) until 6 months (T2)
Participants' satisfaction with minimalist shoes and the various workshops
Time frame: after the 12 intervention sessions (T1) and 6 months (T2).
The number of hours per day that shoes were worn by participants in the experimental group
Time frame: after the 12 intervention sessions (T1) and 6 months (T2).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
20 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Weekly foot health workshops and Balance Workshops in people with Fall Prevention, run by Centre Hospitalier Emile Roux at 20 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 8 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 4 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 20 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The change in the Timed Up and Go test time, expressed in seconds (time frame: at baseline assessment (T0) and after the 12 intervention sessions (T1)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2026.