Postural HygieneNCT07632495
Multicomponent Exercise and Postural Hygiene
A study testing Multicomponent physical exercise with integrated postural hygiene in people with Postural Hygiene, run by Catholic University of Murcia at 1 site in Spain.
Trial summary
This non-randomized clinical study aims to evaluate whether a multicomponent physical exercise program with integrated postural hygiene can improve functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition in adult and older women. Read more about this study
- Who is it for?
- Ages 50 to 82 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Postural Hygiene
- What is being tested?
- Multicomponent physical exercise with integrated postural hygiene
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteSpain
- Study dates
- 30 Jun 2025to 30 Sep 2026
- 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 50 to 82 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Women enrolled in the Maintenance Gymnastics program
- Age between 50 and 82 years.
- Acceptance of participation in the study.
Who cannot join
- Having diseases or conditions that prevent the proper performance of the activity and the assessments.
- Having functional limitations that prevent safe participation in physical activity.
- Having cognitive impairments that hinder understanding of instructions, tests, or questionnaires.
- Refusal to participate in the study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of a Postural Hygiene-Based Physical Exercise Program in Older Adult Women
This non-randomized clinical study aims to evaluate whether a multicomponent physical exercise program with integrated postural hygiene can improve functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition in adult and older women. Eighty participants are allocated to three groups: an experimental group performing exercise with integrated postural hygiene, a reference group with previous postural hygiene training performing the same intervention, and a control group performing the same exercise program without the postural hygiene component. Participants are assessed before, during, and after the intervention, as well as at follow-up. The broader research project also includes a separate cross-sectional observational component designed to describe postural habits, musculoskeletal symptoms, and functional health-related variables in women enrolled in a community-based Maintenance Gymnastics program.
Read the detailed description
The primary component is a non-randomized interventional study with parallel assignment designed to evaluate the effects of a multicomponent physical exercise program integrating postural hygiene strategies. The study is being registered after participant enrollment had started due to an administrative oversight. Data collection is ongoing and has not yet been completed. The intervention protocol, assessment schedule, and outcome measures were defined before completion of data collection and have not been modified based on study findings.
The interventional component includes 80 adult and older women allocated to three groups. The experimental group performs a multicomponent physical exercise program with integrated postural hygiene. The reference group consists of participants who had previously received postural hygiene training and performs the same intervention as the experimental group. The control group performs the same multicomponent physical exercise program without the specific postural hygiene component.
The intervention includes exercises targeting strength, balance, mobility, and postural control. Postural hygiene strategies are integrated throughout exercise practice and are intended to facilitate the transfer of healthy postural behaviors to activities of daily living. These strategies aim to improve postural awareness, movement control, and safer postural habits during functional tasks.
Participants are assessed at four time points: baseline, mid-intervention, post-intervention, and follow-up. Outcomes include functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition. Semi-structured interviews are also conducted to explore perceived changes, program acceptability, postural awareness, and the application of postural hygiene strategies in daily life.
The study is non-pharmacological, non-surgical, and non-invasive. It does not involve drug administration, surgical procedures, invasive techniques, or investigational medical devices. The intervention is delivered by trained instructors following a standardized protocol to ensure consistency across groups.
In addition to the interventional component, the broader project includes a separate cross-sectional observational epidemiological study conducted in a larger sample of women enrolled in the Maintenance Gymnastics program. This component is based exclusively on questionnaire data and aims to describe postural habits, musculoskeletal symptoms, body perception, and variables related to functional health in the target population. It does not include any intervention, group allocation, or follow-up assessments.
- Conditions
- Postural Hygiene
- Being tested
- Multicomponent physical exercise with integrated postural hygiene, Multicomponent physical exercise without postural control
- Keywords
- Multicomponent exercise, Musculoskeletal Pain, Postural Awareness, Older adults, Women, Functional mobility
- Medical subject headings
- Musculoskeletal Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Multicomponent physical exercise with integrated postural hygieneBehavioural
Also called Multicomponent exercise with strength, balance, mobility and postural control, integrating postural hygiene during exercise and daily activities under an instructor-controlled common protocol.
Structured multicomponent physical exercise program including strength, balance, mobility, and postural control exercises, with integrated postural hygiene strategies during exercise execution and activities of daily living. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the two arms with integrated postural hygiene.
Multicomponent physical exercise without postural controlBehavioural
Structured multicomponent physical exercise program including strength, balance, and mobility exercises, delivered without the specific postural control component. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the active comparator arm without postural control.
| Study group | Role | What they receive |
|---|---|---|
| Multicomponent physical exercise with integrated postural hygiene and no prior knowledge | Experimental | Participants without prior postural hygiene knowledge will perform a structured multicomponent physical exercise program with integrated postural hygiene strategies. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. Receives: Behavioral: Multicomponent physical exercise with integrated postural hygiene |
| Multicomponent physical exercise with integrated postural hygiene and prior knowledge | Other | Participants with prior postural hygiene knowledge will perform the same structured multicomponent physical exercise program with integrated postural hygiene strategies as the experimental group. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. Receives: Behavioral: Multicomponent physical exercise with integrated postural hygiene |
| Multicomponent physical exercise without postural control | Active comparator | Participants will perform a structured multicomponent physical exercise program including strength, balance, and mobility exercises, but without the specific postural control component. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. Receives: Behavioral: Multicomponent physical exercise without postural control |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Functional Mobility Assessed Using the Timed Up and Go
The Timed Up and Go (TUG) test assesses functional mobility by measuring the time required for a participant to stand up from a chair, walk 3 meters, turn around, walk back, and sit down. Lower values indicate better functional mobility and balance. Unit of Measure: seconds
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Physical Performance Assessed Using the Short Physical Performance Battery
The Short Physical Performance Battery (SPPB) assesses physical performance using three standardized components: standing balance, usual gait speed, and the chair stand test. The balance assessment includes side-by-side, semi-tandem, and tandem standing positions. Gait speed is evaluated over a short walking distance, and lower-extremity functional strength is assessed using the repeated chair stand test. Each component is scored from 0 to 4 points, and the total score ranges from 0 to 12 points, with higher scores indicating better physical performance. Unit of Measure: Points
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Postural Risk Assessed Using the Rapid Entire Body Assessment
The Rapid Entire Body Assessment (REBA) is an observational ergonomic assessment tool used to evaluate postural risk during functional tasks and movements. The assessment considers body posture, force/load handling, coupling, and activity level by examining the position of the neck, trunk, legs, upper arms, lower arms, and wrists. Total scores range from 1 to 15 points, with higher scores indicating greater postural and musculoskeletal risk and lower scores indicating lower postural risk. Unit of Measure: Points
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Secondary outcomes (5)
Change in Musculoskeletal Symptoms Assessed Using the Nordic Musculoskeletal Questionnaire
The Nordic Musculoskeletal Questionnaire (NMQ) is a standardized questionnaire used to assess the presence and anatomical distribution of musculoskeletal symptoms across body regions, including the neck, shoulders, upper back, lower back, elbows, wrists/hands, hips/thighs, knees, and ankles/feet. The questionnaire records the presence or absence of pain, discomfort, or musculoskeletal symptoms during specified time periods. Results are reported separately for each body region, with a lower prevalence of symptoms indicating a better outcome. Unit of Measure: Presence or absence of musculoskeletal symptoms by body region.
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Health-Related Quality of Life Assessed Using the SF-36 Questionnaire
The 36-Item Short Form Health Survey (SF-36) is a standardized questionnaire used to assess health-related quality of life across eight domains: physical functioning, role limitations due to physical health, bodily pain, general health perceptions, vitality, social functioning, role limitations due to emotional problems, and mental health. Scores are transformed to a scale ranging from 0 to 100 points, with higher scores indicating better perceived health status and quality of life. Unit of Measure: Points
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Body Composition Assessed Using the TANITA BC-401 Monitor
Body composition will be assessed using the TANITA BC-401 body composition monitor. The following parameters will be recorded: body weight (kg), body fat percentage (%), muscle mass (kg), visceral fat (rating), total body water (%), bone mass (kg), and body mass index (kg/m²). Higher muscle mass and total body water values, together with lower body fat percentage, visceral fat and BMI values, indicate improved body composition outcomes following the intervention.
Measured: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Postural Awareness Scale
The Postural Awareness Scale (PAS) is a self-report questionnaire designed to assess an individual's awareness of body posture, body alignment, and postural sensations during daily activities. The scale evaluates conscious perception of body position, muscular tension, and postural adjustments. Higher scores indicate greater postural awareness and improved perception of body posture and movement. Unit of Measure: points
Measured: Baseline
Back Pain and Body Posture Questionnaire
The Back Pain and Body Posture Evaluation Instrument for Adults (BackPEI-A) is a self-administered questionnaire designed to assess back pain prevalence, postural habits, ergonomic behaviors, and lifestyle-related factors associated with spinal health in adults. The questionnaire includes items related to pain frequency and intensity, sitting posture, sleeping posture, backpack or load carrying habits, physical activity, and daily postural behaviors. Higher frequencies of inappropriate postural habits and back pain symptoms indicate poorer spinal health and postural behavior outcomes. Unit of Measure: categorical responses and frequency scores
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jun 2026
- Study start30 Jun 2025
- Primary completion30 Sep 2026 (estimated)
- Study completion30 Sep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Postural HygieneStudies 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
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- This a non-randomized interventional study with three parallel groups: experimental group, reference group, and control group. The experimental group will perform multicomponent physical exercise with integrated postural hygiene. The reference group will consist of participants with previous knowledge of postural hygiene and will perform the same intervention as the experimental group. The control group will perform the same multicomponent physical exercise program, but without the specific postural hygiene component.
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Catholic University of Murcia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Carmen Daniela Quero Calero, Catholic University of Murcia
- Investigators
- Ana I. Rodrigo, Principal investigator, Catholic University of Murcia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07632495
- Sponsor's protocol ID
- CE092506
- Status last verified
- May 2026
- First submitted
- 27 May 2026
- Last updated
- 8 Jun 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: The raw data supporting the conclusions of this intervention will be made available by the investigators, without undule reservación, to and qualified researcher.
Study at a glance
From the registry record, last updated by the sponsor on 8 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of a Postural Hygiene-Based Physical Exercise Program in Older Adult Women
- ClinicalTrials.gov ID
- NCT07632495
- Acronym / sponsor ID
- CE092506
- Conditions
- Postural Hygiene
- Keywords
- Multicomponent exercise, Musculoskeletal Pain, Postural Awareness, Older adults, Women, Functional mobility
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Catholic University of MurciaUniversity, hospital or other
- Study start
- 30 Jun 2025 (actual)
- Primary completion
- 30 Sep 2026 (estimated)
- Study completion
- 30 Sep 2026 (estimated)
- First posted
- 8 Jun 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.
This non-randomized clinical study aims to evaluate whether a multicomponent physical exercise program with integrated postural hygiene can improve functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition in adult and older women. Eighty participants are allocated to three groups: an experimental group performing exercise with integrated postural hygiene, a reference group with previous postural hygiene training performing the same intervention, and a control group performing the same exercise program without the postural hygiene component. Participants are assessed before, during, and after the intervention, as well as at follow-up. The broader research project also includes a separate cross-sectional observational component designed to describe postural habits, musculoskeletal symptoms, and functional health-related variables in women enrolled in a community-based Maintenance Gymnastics program.
Detailed description
The primary component is a non-randomized interventional study with parallel assignment designed to evaluate the effects of a multicomponent physical exercise program integrating postural hygiene strategies. The study is being registered after participant enrollment had started due to an administrative oversight. Data collection is ongoing and has not yet been completed. The intervention protocol, assessment schedule, and outcome measures were defined before completion of data collection and have not been modified based on study findings.
The interventional component includes 80 adult and older women allocated to three groups. The experimental group performs a multicomponent physical exercise program with integrated postural hygiene. The reference group consists of participants who had previously received postural hygiene training and performs the same intervention as the experimental group. The control group performs the same multicomponent physical exercise program without the specific postural hygiene component.
The intervention includes exercises targeting strength, balance, mobility, and postural control. Postural hygiene strategies are integrated throughout exercise practice and are intended to facilitate the transfer of healthy postural behaviors to activities of daily living. These strategies aim to improve postural awareness, movement control, and safer postural habits during functional tasks.
Participants are assessed at four time points: baseline, mid-intervention, post-intervention, and follow-up. Outcomes include functional capacity, postural risk, musculoskeletal symptoms, health-related quality of life, and body composition. Semi-structured interviews are also conducted to explore perceived changes, program acceptability, postural awareness, and the application of postural hygiene strategies in daily life.
The study is non-pharmacological, non-surgical, and non-invasive. It does not involve drug administration, surgical procedures, invasive techniques, or investigational medical devices. The intervention is delivered by trained instructors following a standardized protocol to ensure consistency across groups.
In addition to the interventional component, the broader project includes a separate cross-sectional observational epidemiological study conducted in a larger sample of women enrolled in the Maintenance Gymnastics program. This component is based exclusively on questionnaire data and aims to describe postural habits, musculoskeletal symptoms, body perception, and variables related to functional health in the target population. It does not include any intervention, group allocation, or follow-up assessments.
Study design
- Primary purpose
- Prevention
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 3
- Model description
- This a non-randomized interventional study with three parallel groups: experimental group, reference group, and control group. The experimental group will perform multicomponent physical exercise with integrated postural hygiene. The reference group will consist of participants with previous knowledge of postural hygiene and will perform the same intervention as the experimental group. The control group will perform the same multicomponent physical exercise program, but without the specific postural hygiene component.
| Arm | Type | Receives |
|---|---|---|
| Multicomponent physical exercise with integrated postural hygiene and no prior knowledge | Experimental | Behavioral: Multicomponent physical exercise with integrated postural hygieneParticipants without prior postural hygiene knowledge will perform a structured multicomponent physical exercise program with integrated postural hygiene strategies. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. |
| Multicomponent physical exercise with integrated postural hygiene and prior knowledge | Other | Behavioral: Multicomponent physical exercise with integrated postural hygieneParticipants with prior postural hygiene knowledge will perform the same structured multicomponent physical exercise program with integrated postural hygiene strategies as the experimental group. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. |
| Multicomponent physical exercise without postural control | Active comparator | Behavioral: Multicomponent physical exercise without postural controlParticipants will perform a structured multicomponent physical exercise program including strength, balance, and mobility exercises, but without the specific postural control component. Sessions will follow a previously established common protocol, with the same assessment procedures and time points as the other groups. |
Who may qualify
- Ages
- 50 to 82 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Women enrolled in the Maintenance Gymnastics program
- Age between 50 and 82 years.
- Acceptance of participation in the study.
Key exclusion criteria (4 listed)
- Having diseases or conditions that prevent the proper performance of the activity and the assessments.
- Having functional limitations that prevent safe participation in physical activity.
- Having cognitive impairments that hinder understanding of instructions, tests, or questionnaires.
- Refusal to participate in the study.
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 |
|---|---|---|
| Multicomponent physical exercise with integrated postural hygieneAlso: Multicomponent exercise with strength, balance, mobility and postural control, integrating postural hygiene during exercise and daily activities under an instructor-controlled common protocol.Structured multicomponent physical exercise program including strength, balance, mobility, and postural control exercises, with integrated postural hygiene strategies during exercise execution and activities of daily living. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the two arms with integrated postural hygiene. | Behavioural | Multicomponent physical exercise with integrated postural hygiene and no prior knowledge, Multicomponent physical exercise with integrated postural hygiene and prior knowledge |
| Multicomponent physical exercise without postural controlStructured multicomponent physical exercise program including strength, balance, and mobility exercises, delivered without the specific postural control component. Sessions will be conducted in the usual practice context, following a previously established common protocol and with implementation control by program instructors. This intervention will be assigned to the active comparator arm without postural control. | Behavioural | Multicomponent physical exercise without postural control |
Primary outcome
Change in Functional Mobility Assessed Using the Timed Up and Go
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
The Timed Up and Go (TUG) test assesses functional mobility by measuring the time required for a participant to stand up from a chair, walk 3 meters, turn around, walk back, and sit down. Lower values indicate better functional mobility and balance. Unit of Measure: seconds
Change in Physical Performance Assessed Using the Short Physical Performance Battery
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
The Short Physical Performance Battery (SPPB) assesses physical performance using three standardized components: standing balance, usual gait speed, and the chair stand test. The balance assessment includes side-by-side, semi-tandem, and tandem standing positions. Gait speed is evaluated over a short walking distance, and lower-extremity functional strength is assessed using the repeated chair stand test. Each component is scored from 0 to 4 points, and the total score ranges from 0 to 12 points, with higher scores indicating better physical performance. Unit of Measure: Points
Change in Postural Risk Assessed Using the Rapid Entire Body Assessment
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
The Rapid Entire Body Assessment (REBA) is an observational ergonomic assessment tool used to evaluate postural risk during functional tasks and movements. The assessment considers body posture, force/load handling, coupling, and activity level by examining the position of the neck, trunk, legs, upper arms, lower arms, and wrists. Total scores range from 1 to 15 points, with higher scores indicating greater postural and musculoskeletal risk and lower scores indicating lower postural risk. Unit of Measure: Points
5 secondary outcomes
Change in Musculoskeletal Symptoms Assessed Using the Nordic Musculoskeletal Questionnaire
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Health-Related Quality of Life Assessed Using the SF-36 Questionnaire
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Change in Body Composition Assessed Using the TANITA BC-401 Monitor
Time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)
Postural Awareness Scale
Time frame: Baseline
Back Pain and Body Posture Questionnaire
Time frame: Baseline
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 8 Jun 2026.
- Individual participant dataSharing planned: Yes. The raw data supporting the conclusions of this intervention will be made available by the investigators, without undule reservación, to and qualified researcher.
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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.
Ana I. Rodrigo principal investigator
Catholic University of Murcia
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Multicomponent physical exercise with integrated postural hygiene in people with Postural Hygiene, run by Catholic University of Murcia at 1 site in Spain.
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 4 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: under way, not looking for participants, as of the sponsor's last update on 8 Jun 2026. 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 Spain. 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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Functional Mobility Assessed Using the Timed Up and Go (time frame: Baseline, mid-intervention (4.5 months), post-intervention (9 months), and 6 months after completion of the intervention (15 months from baseline)). The study lists 3 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 8 Jun 2026.