Accidental FallNCT05829369
Intrinsic Foot Muscle Strengthening Interventions for Older Adults
A study testing Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking in people with Accidental Fall, run by Springfield College at 1 site in United States.
Trial summary
Falls are the leading cause of injury in adults over age 65. Muscle weakness in the foot can lead to foot and toe deformities such as collapsed arches or bunions, which have been found to contribute to falls in adults over age 65. Read more about this study
- Who is it for?
- Ages 65 years and olderHealthy volunteers can take part
- Conditions the study is for
- Accidental Fall
- What is being tested?
- Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 90 participants
- Where
- 1 siteUnited States
- Study dates
- 16 Dec 2022to 30 Sep 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
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
- Healthy volunteers accepted
- Older adult
Who may be able to join
- Can ambulate household distances (16 meters) with or without an assistive device
- Have fall risk based on a "yes" to any of the Three Key Questions Do you feel unsteady when standing or walking? Do you worry about falling? Have you fallen in the past year? OR
- Have a fall risk based on Timed Up and Go score (> 12 seconds)
Who cannot join
- poor foot sensation (Semmes-Weinstein)
- lower extremity amputations
- lumbar spine or lower extremity injury or surgery in the past 6 months
- impaired cognitive ability to follow verbal or written instructions (MMSE)
- vestibular disorders
- based on self-report and/or the Vestibular Screening Tool (score > 4)
- participation in a fall prevention program in the previous 6 months
Trial locations and contacts
1 site in 1 country.
United States1 site, 1 recruiting
- Recruiting
Springfield College
Springfield, Massachusetts, 01027
Erin Futrell, 413-748-3590, efutrell@springfieldcollege.edu
About this study
Official title: The Effects of Intrinsic Foot Muscle Strengthening Interventions on Balance, Proprioception, Foot Structure, and Fall Risk in Adults Over Age 65
Falls are the leading cause of injury in adults over age 65. Muscle weakness in the foot can lead to foot and toe deformities such as collapsed arches or bunions, which have been found to contribute to falls in adults over age 65. The current research study aims to investigate the effectiveness of two simple and affordable foot strengthening methods that may make a major impact on balance and fall prevention in older adults.
Read the detailed description
Background: Falls are the leading cause of injury in adults 65 years and older. While causes of falls are multifactorial, foot function plays a vital role. The intrinsic foot muscles (IFM), those that originate and insert within the foot, provide stability and sensory input important for balance. Weakness or disuse of the IFM in older adults can contribute to faulty foot and toe alignment, which have been cited as independent predictors of falls. Wearing minimally cushioned footwear or performing strengthening exercises that target the IFM may improve these muscles' strength, endurance, proprioceptive qualities, and foot/toe structure, which may improve functional mobility and balance in older adults, and thus, prevent falls.
Purpose: The purpose of the proposed research is to analyze the effects of two IFM strengthening interventions (minimal footwear use or strengthening exercises) on IFM strength, proprioception, foot/toe structure, balance and functional mobility, and fall risk in older adults.
Design: Randomized control trial with an effectiveness-implementation hybrid design Type I
Methods: Adults ages > 65 years who can ambulate household distances with or without an assistive device who are determined to be at risk for falls will be invited to participate. Individuals with poor foot sensation, vestibular disorders, lower extremity amputation, injury or surgery to the lower extremities or lumbar spine in the previous 6 months, impaired cognitive ability to follow verbal and written instructions, and those who have participated in a fall prevention program in the past 6 months will be excluded. Following informed consent and initial screening, participants will be randomly allocated to one of three intervention groups (n=90, 30/group):
- intrinsic foot muscle strengthening exercises
- minimal footwear prescribed walking
- control (will receive a fall prevention brochure and seated active motion exercises)
Participants will be encouraged to perform interventions 5 days/week for 16 weeks. After an initial in-person instruction session, participants will have 1 follow-up meeting to review instructions, after which they will receive bimonthly phone calls as a reminder to adhere to the intervention and to record any falls and related details. Participants will be asked to record intervention performance, daily step count (measured by pedometer), and falls in provided diaries. Balance, functional mobility, and fall risk will be measured using the Mini-BesTest, proprioception will be measured using the Lower Extremity Position Test, foot and toe structure will be measured using navicular drop and valgus angle of the 1st metatarsophalangeal joint. Cross sectional area (cm2) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, and quadratus plantae muscles will be measured using ultrasound imaging. Measures regarding balance and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area will occur at baseline, 8 and 16 weeks, and 1 year. Following the 16-week intervention period, participants will be encouraged to continue their intervention twice per week. Ongoing falls diaries and bimonthly phone calls from researchers will occur for 12 months after baseline to record long-term fall rate (falls per person per year). In addition, a process evaluation will be performed regarding participant impressions of the interventions and other study activities to inform future research and clinical implementation.
Data Analysis: a 4 group x 4 time point repeated measures analysis of covariance (ANCOVA) will be used to assess changes in balance, and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area. Falls data will be measured as the rate of falls per person in a 12-month period beginning with the date of the baseline measure, and change in fall risk status will be assessed using Mini-BesTest scores. Implementation data will undergo both quantitative and qualitative analyses.
Significance: Intrinsic foot muscle strengthening interventions have seldom been studied in older adults and their effects and mechanism are not established. This will be the first study to assess the effects of these interventions on proprioception in older adults, the first to use ultrasound imaging measurement following intrinsic foot muscle strengthening in older adults, and the first study to analyze the long-term effects on falls after the performance of these specific interventions. The interventions assessed in this research proposal are simple, safe, and affordable and may have a major impact on functional mobility and reduction of falls for older adults.
- Conditions
- Accidental Fall
- Being tested
- Intrinsic foot muscle strengthening exercises, Minimal footwear with prescribed walking, Control
- Keywords
- older adults, falls, feet, balance, proprioception, muscle strength
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Intrinsic foot muscle strengthening exercisesOther
participants will perform specific toe and foot motions that recruit plantar intrinsic foot muscles, 3 sets of 10 for each exercise, 5 days per week
Minimal footwear with prescribed walkingOther
Participants will be provided minimal footwear. They will walk 30 minutes per day, 5 days per week, and be prescribed a gradual increased time in minimal footwear during daily activities (up to a maximum of 7.5 hours per day).
ControlOther
Participants will perform seated upper and lower extremity active range of motion activities 5 days per week. They will also be given a brochure on fall prevention tips.
| Study group | Role | What they receive |
|---|---|---|
| Intrinsic foot muscle exercise | Experimental | This group will perform intrinsic foot muscle strengthening exercises Receives: Other: Intrinsic foot muscle strengthening exercises |
| Minimal Footwear | Active comparator | This group will perform prescribed walking in and daily wear of minimally cushioned footwear Receives: Other: Minimal footwear with prescribed walking |
| Control | Sham comparator | This group will be given a falls prevention brochure and seated upper extremity and lower extremity active range of motion activities. Receives: Other: Control |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Mini BesTest scores
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Measured: Baseline
Change in Mini BesTest scores
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Measured: 8 weeks post intervention
Change in Mini BesTest scores
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Measured: 16 weeks post intervention
Change in Mini BesTest scores
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Measured: 1 year post intervention
Change in intrinsic foot muscle cross-sectional area/strength
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Measured: Baseline
Change in intrinsic foot muscle cross-sectional area/strength
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Measured: 8 weeks post intervention
Change in intrinsic foot muscle cross-sectional area/strength
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Measured: 16 weeks post intervention
Change in intrinsic foot muscle cross-sectional area/strength
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Measured: 1 year post intervention
Secondary outcomes (12)
Change in hallux valgus angle
a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot
Measured: Baseline
Change in hallux valgus angle
a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot
Measured: 8 weeks post intervention
Change in hallux valgus angle
a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot
Measured: 16 weeks post intervention
Change in hallux valgus angle
a goniometer will be used to measure the angle of the 1st metatarsophalangeal joint of the right foot
Measured: 1 year post intervention
Change in navicular drop measure
the Navicular Drop Test will measure the amount of foot pronation in sitting and standing
Measured: Baseline
Change in navicular drop measure
the Navicular Drop Test will measure the amount of foot pronation in sitting and standing
Measured: 8 weeks post intervention
Change in navicular drop measure
the Navicular Drop Test will measure the amount of foot pronation in sitting and standing
Measured: 16 weeks post intervention
Change in navicular drop measure
the Navicular Drop Test will measure the amount of foot pronation in sitting and standing
Measured: 1 year post intervention
Change in proprioception measure
The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting
Measured: Baseline
Change in proprioception measure
The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting
Measured: 8 weeks post intervetion
Change in proprioception measure
The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting
Measured: 16 weeks post intervention
Change in proprioception measure
The Lower Extremity Proprioception Test will be used to capture proprioception of the foot, ankle, and knee in sitting
Measured: 1 year post intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Apr 2023
- Study start16 Dec 2022
- Primary completion30 Sep 2025 (estimated)
- Study completion30 Sep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Accidental FallStudies 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
- Model description
- Randomized control trial with an effectiveness-implementation hybrid design Type I
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 90 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Springfield College
- Sponsor type
- University, hospital or other
- Collaborators
- Centers for Disease Control and Prevention
- Responsible party
- Sponsor
- Investigators
- Erin Futrell, PhD, Principal investigator, Springfield College
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05829369
- Sponsor's protocol ID
- U01CE003495
- Status last verified
- Apr 2023
- First submitted
- 31 Jan 2023
- Last updated
- 25 Apr 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 25 Apr 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Intrinsic Foot Muscle Strengthening Interventions on Balance, Proprioception, Foot Structure, and Fall Risk in Adults Over Age 65
- ClinicalTrials.gov ID
- NCT05829369
- Acronym / sponsor ID
- U01CE003495
- Conditions
- Accidental Fall
- Keywords
- older adults, falls, feet, balance, proprioception, muscle strength
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Springfield CollegeUniversity, hospital or other
- Collaborators
- Centers for Disease Control and Prevention
- Study start
- 16 Dec 2022 (actual)
- Primary completion
- 30 Sep 2025 (estimated)
- Study completion
- 30 Sep 2025 (estimated)
- First posted
- 25 Apr 2023 (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.
Falls are the leading cause of injury in adults over age 65. Muscle weakness in the foot can lead to foot and toe deformities such as collapsed arches or bunions, which have been found to contribute to falls in adults over age 65. The current research study aims to investigate the effectiveness of two simple and affordable foot strengthening methods that may make a major impact on balance and fall prevention in older adults.
Detailed description
Background: Falls are the leading cause of injury in adults 65 years and older. While causes of falls are multifactorial, foot function plays a vital role. The intrinsic foot muscles (IFM), those that originate and insert within the foot, provide stability and sensory input important for balance. Weakness or disuse of the IFM in older adults can contribute to faulty foot and toe alignment, which have been cited as independent predictors of falls. Wearing minimally cushioned footwear or performing strengthening exercises that target the IFM may improve these muscles' strength, endurance, proprioceptive qualities, and foot/toe structure, which may improve functional mobility and balance in older adults, and thus, prevent falls.
Purpose: The purpose of the proposed research is to analyze the effects of two IFM strengthening interventions (minimal footwear use or strengthening exercises) on IFM strength, proprioception, foot/toe structure, balance and functional mobility, and fall risk in older adults.
Design: Randomized control trial with an effectiveness-implementation hybrid design Type I
Methods: Adults ages > 65 years who can ambulate household distances with or without an assistive device who are determined to be at risk for falls will be invited to participate. Individuals with poor foot sensation, vestibular disorders, lower extremity amputation, injury or surgery to the lower extremities or lumbar spine in the previous 6 months, impaired cognitive ability to follow verbal and written instructions, and those who have participated in a fall prevention program in the past 6 months will be excluded. Following informed consent and initial screening, participants will be randomly allocated to one of three intervention groups (n=90, 30/group):
- intrinsic foot muscle strengthening exercises
- minimal footwear prescribed walking
- control (will receive a fall prevention brochure and seated active motion exercises)
Participants will be encouraged to perform interventions 5 days/week for 16 weeks. After an initial in-person instruction session, participants will have 1 follow-up meeting to review instructions, after which they will receive bimonthly phone calls as a reminder to adhere to the intervention and to record any falls and related details. Participants will be asked to record intervention performance, daily step count (measured by pedometer), and falls in provided diaries. Balance, functional mobility, and fall risk will be measured using the Mini-BesTest, proprioception will be measured using the Lower Extremity Position Test, foot and toe structure will be measured using navicular drop and valgus angle of the 1st metatarsophalangeal joint. Cross sectional area (cm2) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, and quadratus plantae muscles will be measured using ultrasound imaging. Measures regarding balance and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area will occur at baseline, 8 and 16 weeks, and 1 year. Following the 16-week intervention period, participants will be encouraged to continue their intervention twice per week. Ongoing falls diaries and bimonthly phone calls from researchers will occur for 12 months after baseline to record long-term fall rate (falls per person per year). In addition, a process evaluation will be performed regarding participant impressions of the interventions and other study activities to inform future research and clinical implementation.
Data Analysis: a 4 group x 4 time point repeated measures analysis of covariance (ANCOVA) will be used to assess changes in balance, and functional mobility, proprioception, foot/toe structure, and muscle cross sectional area. Falls data will be measured as the rate of falls per person in a 12-month period beginning with the date of the baseline measure, and change in fall risk status will be assessed using Mini-BesTest scores. Implementation data will undergo both quantitative and qualitative analyses.
Significance: Intrinsic foot muscle strengthening interventions have seldom been studied in older adults and their effects and mechanism are not established. This will be the first study to assess the effects of these interventions on proprioception in older adults, the first to use ultrasound imaging measurement following intrinsic foot muscle strengthening in older adults, and the first study to analyze the long-term effects on falls after the performance of these specific interventions. The interventions assessed in this research proposal are simple, safe, and affordable and may have a major impact on functional mobility and reduction of falls for older adults.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 3
- Model description
- Randomized control trial with an effectiveness-implementation hybrid design Type I
| Arm | Type | Receives |
|---|---|---|
| Intrinsic foot muscle exercise | Experimental | Other: Intrinsic foot muscle strengthening exercisesThis group will perform intrinsic foot muscle strengthening exercises |
| Minimal Footwear | Active comparator | Other: Minimal footwear with prescribed walkingThis group will perform prescribed walking in and daily wear of minimally cushioned footwear |
| Control | Sham comparator | Other: ControlThis group will be given a falls prevention brochure and seated upper extremity and lower extremity active range of motion activities. |
Who may qualify
- Ages
- 65 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Older adult
Key inclusion criteria (3 listed)
- Can ambulate household distances (16 meters) with or without an assistive device
- Have fall risk based on a "yes" to any of the Three Key Questions Do you feel unsteady when standing or walking? Do you worry about falling? Have you fallen in the past year? OR
- Have a fall risk based on Timed Up and Go score (> 12 seconds)
Key exclusion criteria (7 listed)
- poor foot sensation (Semmes-Weinstein)
- lower extremity amputations
- lumbar spine or lower extremity injury or surgery in the past 6 months
- impaired cognitive ability to follow verbal or written instructions (MMSE)
- vestibular disorders
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 |
|---|---|---|
| Intrinsic foot muscle strengthening exercisesparticipants will perform specific toe and foot motions that recruit plantar intrinsic foot muscles, 3 sets of 10 for each exercise, 5 days per week | Other | Intrinsic foot muscle exercise |
| Minimal footwear with prescribed walkingParticipants will be provided minimal footwear. They will walk 30 minutes per day, 5 days per week, and be prescribed a gradual increased time in minimal footwear during daily activities (up to a maximum of 7.5 hours per day). | Other | Minimal Footwear |
| ControlParticipants will perform seated upper and lower extremity active range of motion activities 5 days per week. They will also be given a brochure on fall prevention tips. | Other | Control |
Primary outcome
Change in Mini BesTest scores
Time frame: Baseline
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Change in Mini BesTest scores
Time frame: 8 weeks post intervention
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Change in Mini BesTest scores
Time frame: 16 weeks post intervention
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Change in Mini BesTest scores
Time frame: 1 year post intervention
a comprehensive measure of balance, gait, and functional mobility (max score 28 and indicates good balance/mobility and low fall risk)
Change in intrinsic foot muscle cross-sectional area/strength
Time frame: Baseline
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Change in intrinsic foot muscle cross-sectional area/strength
Time frame: 8 weeks post intervention
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Change in intrinsic foot muscle cross-sectional area/strength
Time frame: 16 weeks post intervention
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
Change in intrinsic foot muscle cross-sectional area/strength
Time frame: 1 year post intervention
real-time ultrasound imaging will measure muscle size (cross-sectional area) of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, quadratus plantae, and abductor digiti minimi muscles of the right foot
12 secondary outcomes
Change in hallux valgus angle
Time frame: Baseline
Change in hallux valgus angle
Time frame: 8 weeks post intervention
Change in hallux valgus angle
Time frame: 16 weeks post intervention
Change in hallux valgus angle
Time frame: 1 year post intervention
Change in navicular drop measure
Time frame: Baseline
Change in navicular drop measure
Time frame: 8 weeks post intervention
Change in navicular drop measure
Time frame: 16 weeks post intervention
Change in navicular drop measure
Time frame: 1 year post intervention
Change in proprioception measure
Time frame: Baseline
Change in proprioception measure
Time frame: 8 weeks post intervetion
Change in proprioception measure
Time frame: 16 weeks post intervention
Change in proprioception measure
Time frame: 1 year post intervention
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Apr 2023.
- Individual participant dataSharing planned: Undecided
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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. This study is not recruiting at the moment.
Erin Futrell, PhD principal investigator
Springfield College
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intrinsic foot muscle strengthening exercises and Minimal footwear with prescribed walking in people with Accidental Fall, run by Springfield College at 1 site in United States.
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 3 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: status not confirmed, as of the sponsor's last update on 25 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. 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. Some participants in this study may receive a placebo. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Erin Futrell, PhD (413-748-3590, efutrell@springfieldcollege.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Mini BesTest scores (time frame: Baseline). The study lists 8 primary outcomes in all. 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 25 Apr 2023.