ObesityNCT06475092
Relation Between Muscle Mass, Total Body Fat, Visceral Fat, Waist Hip Ratio and Sleeping Hours in Patient With Nonspecific Back Pain
An observational study of Obesity and Back Pain, run by Ahram Canadian University at 1 site in Egypt.
Trial summary
Objective: To find out if there are a relation between muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours in patient with nonspecific back pain. Design: Cross sectional study. Read more about this study
- Who is it for?
- Ages 20 to 40 yearsHealthy volunteers can take part
- What is being tested?
- Tanita device
- How many people
- 30 participants
- Where
- 1 siteEgypt
- Study dates
- 26 Jun 2024to 30 Jul 2024
- Phase
- Observational
- 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 20 to 40 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: 30 male and female patient, Their ages will range from 20-40 years old. All of them suffer from mild to moderate degree of low back pain. and they complain from low back pain for 1 month ago
Who may be able to join
- •adulthood with low back pain
- Their ages will range from 20-40 years old.
- All of them suffer from mild to moderate degree of low back pain.
- The subjects complain from low back pain for 1 month ago
Who cannot join
- Exclusion criteria were a history of any of the following condition:
- inflammatory diseases or any rheumatic disorders,
- a history of vertebral fractures
- surgical spinal fixation.
- •any neurological disorders like MS
Trial locations and contacts
1 site in 1 country.
About this study
Objective: To find out if there are a relation between muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours in patient with nonspecific back pain.
Design: Cross sectional study. Subjects: 30 male and female patients with age ranged from 25 to 40 years old diagnosed as nonspecific low back pain will participate in this study.
Main measures: the Outcome measures will be including the assessment of muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours.
Results: The results will be analyzed via co relation test.
Read the detailed description
Objective: To find out if there are a relation between muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours in patient with nonspecific back pain.
methods:
- tatinia bioelectric impedance device used for measurement of muscle mass total body fat and visceral fat
- waist hip ratio measured by tape measurement The waist-hip ratio or waist-to-hip ratio (WHR) is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement (W⁄H). participants 30 male and female patient will participate in this study
- Being tested
- Tanita device
- Medical subject headings
- Obesity, Back Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tanita deviceOther
Also called tap measurement
bioelectric impedance analysis
What is being measured
The primary outcome is the main question the study is designed to answer.
Tanita device will be used for measurement of total body fat , muscle mass and visceral fat
bioelectric impedance analysis device will be used for assessment of total body fat ,muscle mass and viseral fat
Measured: baseline
Waist hip ratio will be measured by tape measurement
The waist-hip ratio or waist-to-hip ratio (WHR) is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement (W⁄H).
Measured: base line
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jun 2024
- Study start26 Jun 2024
- Primary completion30 Jul 2024
- Study completion30 Jul 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ObesityStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ahram Canadian University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mohamed Ababa, Ahram Canadian University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06475092
- Sponsor's protocol ID
- P.T-ORT 06/2024-546
- Status last verified
- Sep 2024
- First submitted
- 11 Jun 2024
- Last updated
- 5 Sep 2024
- 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 5 Sep 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Relation Between Muscle Mass, Total Body Fat, Visceral Fat, Waist Hip Ratio and Sleeping Hours in Patient With Nonspecific Back Pain
- ClinicalTrials.gov ID
- NCT06475092
- Acronym / sponsor ID
- P.T-ORT 06/2024-546
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Ahram Canadian UniversityUniversity, hospital or other
- Study start
- 26 Jun 2024 (actual)
- Primary completion
- 30 Jul 2024 (actual)
- Study completion
- 30 Jul 2024 (actual)
- First posted
- 26 Jun 2024 (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.
Objective: To find out if there are a relation between muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours in patient with nonspecific back pain.
Design: Cross sectional study. Subjects: 30 male and female patients with age ranged from 25 to 40 years old diagnosed as nonspecific low back pain will participate in this study.
Main measures: the Outcome measures will be including the assessment of muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours.
Results: The results will be analyzed via co relation test.
Detailed description
Objective: To find out if there are a relation between muscle mass, total body fat, visceral fat, waist hip ratio and sleeping hours in patient with nonspecific back pain.
methods:
- tatinia bioelectric impedance device used for measurement of muscle mass total body fat and visceral fat
- waist hip ratio measured by tape measurement The waist-hip ratio or waist-to-hip ratio (WHR) is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement (W⁄H). participants 30 male and female patient will participate in this study
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 20 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- 30 male and female patient, Their ages will range from 20-40 years old. All of them suffer from mild to moderate degree of low back pain. and they complain from low back pain for 1 month ago
Key inclusion criteria (4 listed)
- •adulthood with low back pain
Key exclusion criteria (5 listed)
- inflammatory diseases or any rheumatic disorders,
- a history of vertebral fractures
- surgical spinal fixation.
- •any neurological disorders like MS
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 |
|---|---|---|
| Tanita deviceAlso: tap measurementbioelectric impedance analysis | Other | – |
Primary outcome
Tanita device will be used for measurement of total body fat , muscle mass and visceral fat
Time frame: baseline
bioelectric impedance analysis device will be used for assessment of total body fat ,muscle mass and viseral fat
Waist hip ratio will be measured by tape measurement
Time frame: base line
The waist-hip ratio or waist-to-hip ratio (WHR) is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement (W⁄H).
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Sep 2024.
- 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. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Obesity and Back Pain, run by Ahram Canadian University at 1 site in Egypt.
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 4 inclusion and 5 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: finished, as of the sponsor's last update on 5 Sep 2024. 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 Egypt. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Tanita device will be used for measurement of total body fat , muscle mass and visceral fat (time frame: baseline). The study lists 2 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 5 Sep 2024; AzTrials last refreshed its copy on 7 Nov 2026.