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Comparison of a Weight Bearing and a Non-weight Bearing Protocol on Osteoporotic Women With Chronic Low Back Pain

Comparison of the Effect of a Weight Bearing Protocol and a Non-weight Bearing Protocol on Osteoporotic Women With Chronic Low Back Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03747289
Enrollment
53
Registered
2018-11-20
Start date
2018-12-20
Completion date
2021-02-22
Last updated
2021-08-17

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

Conditions

Low Back Pain, Osteoporosis

Brief summary

The effect of exercising in different body positions on bone growth in osteoporotic women is known, but its effect on their function, low back pain, lumbar range of motion and quality of life remains unknown. Therefore, the investigators plan to make a comparison of the effect of a weight bearing protocol and a non-weight bearing protocol on osteoporotic women with chronic low back pain. 40 women with osteoporosis and low back pain will be divided into two groups. Each group will be given a specific exercise protocol, twice a week for four weeks, 45 minutes each time. The participants will be tested before starting the program, immediately after finishing it and again two months later. The tests will include filling out the Roland Morris Disability Questionnaire, the SF-36 quality of life Questionnaire, pain measurement by VAS (Visual Analogue Scale) and lumbar range of motion measurement by a digital Inclinometer. Statistical analysis will be made in order to compare the dependent variables between groups.

Detailed description

40 women with osteoporosis and low back pain will be recruited by referral of doctors to the physical therapy clinic in Bat-Yam, Israel. Each woman will be tested by one investigator after meeting the criteria of eligibility and after obtaining formed consent . The tests will include filling out the Roland Morris Disability Questionnaire, the SF-36 quality of life Questionnaire, pain measurement by VAS and lumbar range of motion measurement by a digital Inclinometer. By order of appearance, each participant will be assigned to one of two groups - weight bearing group or non-weight bearing group. After recruiting at least 3 participants in each group, a different investigator will begin a specific exercise protocol for each of the groups for four weeks - twice a week, 45 minutes each time, a total of 8 sessions. After each participant finishes all 8 sessions, she will be tested for the second time by the first investigator, the same tests as the first time. A third identical test will be preformed two months after finishing the program. After all the participants finish the program statistical analysis will be made in order to compare the dependent variables between groups.

Interventions

OTHERperforming exercises in a weight bearing posture

20 participants will perform exercises in a weight bearing posture

OTHERperforming exercises in a non weight bearing posture

20 participants will perform exercises in a non weight bearing posture

Sponsors

Bait Balev Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

the investigator will check all the participants without knowing to which group they are assigned to

Eligibility

Sex/Gender
FEMALE
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* women with osteoporosis (T score lower than -2.5) * women whom had suffered from non specific low back pain for the last 3 months or more.

Exclusion criteria

* history of operations in the spine * history of cancer or neurologic disease * history of fractures * previous trauma to the spine * persons whom for any reason cannot sit on a chair or lie on a mattress for 45 minutes

Design outcomes

Primary

MeasureTime frameDescription
Change of physical disability3 monthsthe Roland Morris Disability Questionnaire. The score of the questionnaire is the total number of items checked - i.e. from a minimum of 0 to a maximum of 24.

Secondary

MeasureTime frameDescription
change in lumbar range of motion - flexion and extension3 monthsdigital inclinometer. The change will be assessed by the difference in number of degrees measured
change in pain intensity3 monthsVisual Analogue Scale (VAS). A scale from 0 (no pain) to 10 (the worst possible pain)
change in health related quality of life3 monthsthe Short Form-36 (SF-36) quality of life Questionnaire. A questionnaire of 36 questions, each response receives a specific value

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026