Skip to content

The effect of HMB supplementation on spinal canal stenosis

The effect of core stability training with Beta-Hydroxy Beta-Methyl Butyrate (HMB) supplementation on pain, function and strength of lumbar muscles in patients with spinal canal stenosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201130049546N1
Enrollment
50
Registered
2020-12-17
Start date
2020-03-20
Completion date
Unknown
Last updated
2021-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

spinal canal stenosis. Spinal stenosis

Interventions

Intervention 1: Intervention group: The intervention includes an educational and treatment package containing training on how to sit and sleep properly, giving information about adapting to pain, teac

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 45 years Having a clinical history with diagnostic imaging evidence (CT or MRI) indicating lumbar spinal canal stenosis Decreased walking ability associated with lumbar spinal canal stenosis Ability to refer to receive a treatment plan Ability to do low-intensity exercise Ability to walk up to twenty meters without the need for assistive devices No history of cancer, high weight loss in recent months No history of neurogenic disease such as stroke, cervical myelopathy or neurodegenerative disease including Parkinson's disease in addition to lumbar spinal canal stenosis that affects walking Willingness to participate in the study

Exclusion criteria

Exclusion criteria: Symptoms of cauda equina, such as saddle anesthesia Incidence of neurogenic disease such as stroke, cervical myelopathy or neurodegenerative disease including Parkinson's disease that affects a person's gait. Dangerous symptoms such as fever, nocturnal pain, lack of urinary and fecal control, progressive movement disorder in the lower extremities Surgery for lumbar spinal canal stenosis or lumbar spine fusion is performed during the study after collecting the required initial information.

Design outcomes

Primary

MeasureTime frame
Pain is a quantitative variable measured by the Visual Analogue Scale. Timepoint: Variable measurement at the beginning of the study before the intervention and 6 weeks after the intervention. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Ability to perform daily activities. Timepoint: Before the intervention and 6 weeks after the intervention. Method of measurement: Oswestry Disability Index.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmehran yousefi

Tehran University of Medical Sciences

mehr.yousefi1367@gmail.com+98 21 6691 0301

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026