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Lumbar Spinal StenosisPAESPNCT04079894

Physical Activity in the Elderly Spine Patient

An observational study of Lumbar Spinal Stenosis and Low Back Pain, run by Malin Eleonora av Kák Gustafsson, MD at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Purpose Physical activity reduces the risk of several diseases of the body and the mind1, 2 and can help the elderly maintain physical abilities and self-efficacy in daily life1. Read more about this study

Who is it for?
Ages 60 years and olderHealthy volunteers can take part
Conditions the study is for
Lumbar Spinal Stenosis, Low Back Pain
What is being tested?
Standard Movement Protocol and Accerelerometer Monitoring
Type of treatment
Medical device
How many people
206 participants
Where
1 siteDenmark
Study dates
26 Jun 2019to 1 Feb 2023
How long will I take part?
3 Months
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 60 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The study will include patients with LSS on a degenerative basis, age >=60, referred to the spine center by primary or secondary health care, in the Region of Southern Denmark. Patients with Low Back Pain will be included from three chiropractic clinics in the Region of Southern Denmark. Healthy participants will be identified among hospital staff, acquaintances and participating patients' spouse/acquaintances.

Who may be able to join

  • Informed written consent.
  • Fluent in Danish in reading and speaking.
  • Age >60 with LSS, +/- spondylolisthesis diagnosed via clinical examination and MRI. Suffering from neurogenic claudication with positive answers to a set of six items characteristic to LSS[29].
  • Patients in phase A will be included to represent a spectrum of severeness of LSS and age. Severeness will be evaluated by ODI score, VAS and self-reported maximum walking distance.
  • Patients for phase C will have the additional inclusion criteria of being scheduled for decompressive surgery.

Who cannot join

  • Other disease limiting walking rather than neurogenic claudication, such as cardiopulmonary diseases, vascular claudication, recent operation or fracture of spine, pelvis or leg, severe hip or knee arthrosis (not efficiently threated by hip/knee replacement), systemic muscular diseases, impaired vision.
  • Traits which interfere with the participants' gait pattern, such as habitual use of walking aids during walking at home and away from home, drop foot.
  • Eligibility Criteria for Patients with LBP:
  • Informed written consent.
  • Fluent in Danish in reading and speaking.
  • Age >60
Show all 10Show fewer
  • Suffering from Low Back Pain
  • Low Back Pain is the primary source of pain and disability.
  • Eligibility Criteria for Healthy Participants:
  • Healthy participants will be >60 years old and have the same exclusion criteria as patients, with the addition of not suffering from neurogenic claudication.

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Spine Centre of Southern Denmark

    Middelfart, 5500

Other trials in Denmark

About this study

Purpose Physical activity reduces the risk of several diseases of the body and the mind1, 2 and can help the elderly maintain physical abilities and self-efficacy in daily life1. The overall purpose of the project is to provide clinicians with a tool to objectively assess physical activity in daily life and thus provide an informed basis for individualized care of elderly patients with spine disease. We would like to introduce this tool to a broad population of elderly patients with low back pain to give an overview of the range and variability in physical activity. We will also look into a method for accurate step count in spine disorders where patients have severe walking impairment due to affected lumbar nerve roots.

Read the detailed description

Background Spine disorders, such as low back pain, come with considerable physical limitations, and participation in social events and everyday life can be burdensome2. Efforts to increase physical ability and involvement in everyday life are essential to maintain or heighten quality of life in spite of chronic pain.

Some spine disorders can negatively affect lumbar nerve roots, where the symptoms radiate to the legs. Lumbar Spinal Stenosis (LSS) is one of many chronic spinal pain syndromes, with specific structural abnormalities that can be detected on MRI scans, including narrowing of the spinal canal. Its clinical presentation involves radiation of pain and sensory disturbance to buttocks and legs while walking3. Although there is considerable variation in the diagnostic criteria used, spinal stenosis is common in the elderly, and a recent review reported prevalences between 11% and 38% depending on criteria and study population4. The disease considerably constrains patients' walking ability, which means that patients experience problems with exercise and leisure activities5. Physical activity is significantly reduced, and a recent study shows that individuals with LSS spend 82% of their day sitting or lying down, compared to 35% in healthy adults over 60 years6, leading to an increase in lifestyle diseases such as hypertension7.

Thus, the aging patient with a spine disorder such as LSS or low back pain has to cope with the functional limitations of their disease, as well as the natural decline of function with age1. It is therefore very important for this group of patients that healthcare providers can support their pursuit of an active life. In order to do so, it is necessary for healthcare providers to have reliable knowledge about the individual patients' physical activity and functional impairment in daily life. Such information is typically collected through interviews, physical exams, questionnaires, and the occasional objective test, which only provide indirect, predominantly subjective, information about physical activity in everyday life.

Emerging technology in the form of wearable sensors is breaking new ground and becoming more widespread. Existing research has used sensors such as accelerometers to quantify and differentiate time spent standing, walking, cycling, and sitting or lying down, with high accuracy8. Previous studies have already established that accelerometer-based step counts in elderly people are accurate9-13, but they are influenced by 1) the physical location of the accelerometer on the body14, 15, 2) the method used to transform raw accelerometer data16, and 3) traits of the person wearing it, such as gait speed, use of assistive devices, and age17. As LSS can alter gait characteristics18 and can give severe walking impairment, accelerometer measures of step count developed for healthy adults could be inaccurate in these patients. Since walking impairment is the most prominent disability in LSS, we see the need for a tested and valid measure of walking activity in daily living.

The study consists of two parts, each with a corresponding aim: Part I) develop and examine the validity of an accelerometer-based method of measuring walking activity in daily living in patients with LSS. Part II) uncover objectively identifiable profiles of physical activity in elderly patients with LSS and/or low back pain.

Methods Part I is a method development and validation study containing projects A, B and C.

Project A: Develop an accelerometer-based method of step count for patients with LSS and evaluate its accuracy by comparing it to a gold standard.

Project B: Evaluate the construct validity of the developed method in a free-living environment.

Project C: Evaluate the responsiveness of the developed method. Part II is a cross-sectional cohort study containing projects D, E and F. Project D: Quantify the amount of time spent standing, walking, cycling, and sitting/lying down in patients with confirmed LSS in secondary care.

Project E: Quantify the amount of time spent standing, walking, cycling, and sitting/lying down in patients with low back pain in chiropractic primary care.

Project F: Compare physical activity in LSS and low back pain patients to a randomly selected population of individuals 60 years of age or more.

Part I Project A- Gold standard Project A of the project is completed. Thirty (n=30) patients with lumbar spinal stenosis were included. To investigate the most optimal bodily location to place the accelerometer, each participant wore five accelerometers in different locations: the wrist, thigh, ankle, hip, and lower back, while going through a standardized movement protocol that involved walking, sitting down and standing up, cycling, and walking with walking aids. For validation against a gold standard, we recorded the standardized movement protocol on video and compared the accelerometer data to the actual observed activity on the recordings. An algorithm for quantifying the step count in the accelerometer data was developed based on data from the first 15 patients. The agreement and relationship between the gold standard and accelerometer step count was evaluated for each body location. The correlation between accelerometer step count and manually counted steps were 0.99-1.00 during continuous walking for all bodily locations. They were diminishing but still satisfactory while using a rollator for accelerometers placed on the ankle (0.98) and thigh (0.72). False steps were detected during cycling, but it is possible to correct this with an accelerometer placed on the thigh.

Project B- Construct validity Ninety-five (n=95) patients with lumbar spinal stenosis will be included and wear a single Axivity accelerometer on the thigh for seven days during their normal everyday life. Twenty patients (n=20) will be asked to wear a StepWatch on the right ankle simultaneously. In addition, we gather clinical data, ask participants to perform a Self-Paced Walk Test (SPWT), complete questionnaires and fill out a small walking diary for each day in the week. Please see Appendix I for the questionnaires.

The accelerometer data from patients in project B will be analyzed exploratively, and the raw accelerometer data will be transformed into relevant measures of walking performance, including the number of steps taken per day and the length of continuous walking in minutes.

From the data collected and walking measures calculated, face validity and construct validity will be examined in accordance to the methods suggested by de Vet et al19. The primary hypothesis concerns the correlation between the SPWT results and the accelerometer measures.

Project C- Responsiveness Measures of walking ability has been documented to improve in patients with LSS after surgery20, 21. The patients from project B who after inclusion have had spine surgery to relieve symptoms of lumbar spinal stenosis will be invited to come to the clinic for a follow-up three months after surgery. At follow-up we will repeat the accelerometer measures, walk test, and questionnaires performed in project B. This will enable us to test correlation between change scores in accelerometer measures, walk test and questionnaires and thereby determine whether the accelerometer measures can detect change after surgery.

Part II Project D- Physical activity and lumbar spinal stenosis The raw accelerometer data collected from patients with lumbar spinal stenosis in project B will be used for the purpose stated in project B, as well as to quantify the amount of time spent standing, walking, cycling, and sitting/lying down.

Project E- Physical activity and low back pain One-hundred-and-ten patients with low back pain from chiropractic clinics will be included. The patient will be invited to participate by their chiropractor as part of their visit to the clinic. Clinic personnel will place an accelerometer on the thigh of the patient on the day of inclusion. The patient will be instructed to wear the accelerometer for seven days before returning it to the clinic. Upon return, clinic personnel will download the raw accelerometer data from the accelerometer and upload it to a research database. Questionnaires on pain, function, life quality, and clinical data will be sent to the patient electronically. The chiropractic clinic will be financially compensated for their involvement. The uploaded raw accelerometer data will be analyzed to determine the amount of time spent standing, walking, cycling, and sitting/lying down per day.

Project F- Comparison to background population We will seek to compare the physical activity of patients to individuals 60 years of age or more from the Lolland-Falster Health Study. Participants in the Lolland-Falster Health Study have been randomly selected from the population of Lolland-Falster and have had accelerometer-data collected during every-day life using the same brand accelerometer, Axivity, as in the other parts of this protocol. Data on the participants will be requested from the Lolland-Falster Health Study Steering Committee.

Study population The study will include two study populations from the Region of Southern Denmark. The first population consists of 125 patients with LSS referred from primary or secondary care to the Spine Centre of Southern Denmark, Middelfart. Lumbar spinal stenosis is to be diagnosed via clinical examination and MRI, with pain when walking and relief of pain upon sitting down (neurogenic claudication) with positive answers to a set of six items characteristic to lumbar spinal stenosis22.

The second population consists of 110 patients from chiropractic clinics. The patients suffer from low back pain, with or without radiating pain to the legs.

In addition to their diagnosis, the following eligibility criteria apply to both study populations:

Inclusion criteria:

Age 60 or above. Fluent in Danish.

Exclusion criteria:

Other disease that limit physical activity rather than the patient's spine disorder, such as severe cardiopulmonary diseases; vascular claudication; recent operation or fracture of the spine, pelvis or leg; hip or knee arthrosis (not efficiently treated by hip/knee replacement); systemic muscular diseases; severely impaired vision; wheelchair use; disabling systemic disease.

Dementia. Accelerometry The accelerometer used in this study will be Axivity AX6 and AX3, which has been shown to be valid and accurate with step detection in healthy adults23, 24. The Axivity AX6 is small (2 x 3 x 1 cm), lightweight, offers access to raw accelerometer data, and will be fastened to the skin using a hypo-allergic band-aid. The accelerometer is waterproof and the battery will keep for the full week, and consequently patients do not need to attend to it but can go about their daily lives as they usually would. The algorithm used to detect physical activity will be the method developed by Skotte et al8, and the step detection algorithm developed in this project is a modified version of the algorithm proposed by Hickey et al25. Monitoring will be planned not to take place during larger activities not usually part of their habitual routines, such as trips to foreign countries or holidays.

Sample Size and Statistical Analysis Sample size in project A was 30 patients since this is the recommended number when developing algorithms26 and was sufficient to show a statistically significant two-tailed correlation of 0.5 or higher.

Correlation between questionnaires of pain and function (The Oswestry Disability Index, The ODI) and accelerometer measured step count and continuous walking has been shown to range from around 0.3 to 0.5. Walking tests have been shown to correlate above 0.5 with the ODI27. A sample size of 85 patients is needed to show a correlation of 0.3 or higher as significantly different from 0, with p<0.05 and power of 80%. Therefore, when testing hypotheses of relations between measurements in project B, with ten extra patients to account for drop-outs and missing data, the sample size will be 95.

97 patients from chiropractic clinics will be sufficient to calculate measures that are 95% likely to lie within ten percent of the true population value. An extra 13 patients will be included to account for drop-outs and missing data.

Physical activity will be described by the number of minutes spent in the categories of standing, walking, cycling, and sitting/lying.

Description and statistical analysis of data will be made using the R software. Parametric tests of correlation and difference between means will be used if data are described as normally distributed or following a t-distribution. Ordinal data or data not described as normally distributed will be analyzed using non-parametric statistics.

Facilities and Organization Data will be collected from both private chiropractic practice and the Spine Centre of Southern Denmark, Lillebælt Hospital, Middelfart, where more than 1000 patients are diagnosed with lumbar spinal stenosis each year. Approximately 300 of these undergo surgery for the condition.

Ph.D. student Malin Eleonora av Kák Gustafsson, M.D., will be conducting the study as principal investigator. Malin Eleonora av Kák Gustafsson is part of the spine clinic team in Middelfart and will be responsible for the inclusion of participants, data gathering and statistical analyses. The Ph.D. student will administer the walk test in patients with lumbar spinal stenosis. A research assistant and secretary at the spine center will assist in scheduling patient appointments, gathering questionnaires and accelerometers, and provide support to chiropractor clinics.

The main supervisor is Søren O´Neill, Assoc. Professor, Ph.D., M.Rehab. He is head of research at the Spine Centre of Southern Denmark and has several years of experience in supervising Ph.D. students and performing clinical research in spine diseases.

Co-supervisors are Niels Wedderkopp, M.D., Clinical Professor, Ph.D., Jan Christian Brønd, MSc, postdoc, PhD and Berit Schiøttz-Christensen M.D., professor, Ph.D. Niels Wedderkopp contributes with extensive knowledge on applying and interpreting accelerometer monitoring in clinical research and many years of experience in planning and executing methodologically sound clinical research and work with patients with musculoskeletal degenerative disorders.

Jan Christian Brønd is a postdoc focusing on developing accelerometer measurements of physical activity. He has an engineering background and more than 20 years of experience in software development, and a PhD in health sciences. Jan Christian Brønd will be developing and optimizing the model in phase A.

Berit Schiøttz-Christensen provides the project with a thorough insight into low back pain and spinal stenosis in the primary and secondary sectors and ensures a clinically relevant approach for the measurement method.

Timeline The study will take three years to complete and is planned to finish in October 2023. Project A is finished. The inclusion of patients in project B and follow-up as described in project C is ongoing and will be finished in February 2023. Forty-two of the 95 patients in project B have been included. The inclusion of patients in chiropractic care is planned to start in August 2022 and be completed in March 2023. The last months are reserved for data analysis, publication of articles, dissemination, and Ph.D. thesis.

Ethics and Approvals The study will be conducted in accordance with the Helsinki-II declaration and principles of oral and written consent. Part I of the study has been presented to the Ethical Committees of the Region of Southern Denmark, who has decided that there is no obligation to notify the committees of this project. We expect their assessment regarding the patients in chiropractic care to be in hand in March 2022. Information on all processing of personal data in this project will be added to the records of the Region of Southern Denmark according to the GDPR article 30.

Expected Outcomes of the Study and Clinical Relevance We expect the accelerometer measure to be a feasible and valid measure of physical activity in daily living, including walking activity. The measure is expected to be sensitive enough to detect changes over time, helping patients and caregivers evaluate treatments, stay tuned, and put in extra effort when needed. The method will be well described and accessible for all interested parties, ready for incorporation into user-friendly, self-administered applications. Furthermore, the accelerometer method is expected to stimulate further research into its diagnostic possibilities and prognostic uses.

Being tested
Standard Movement Protocol, Accerelerometer Monitoring
Keywords
Accelerometry, Walking, Physical Activity, Sedentary time
Medical subject headings
Spinal Stenosis, Low Back Pain, Motor Activity, Sedentary Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Standard Movement ProtocolOther

    Participant walking, cycling and sitting according to a pre-specified protocol.

  • Accerelerometer MonitoringDevice

    7 days of accelerometer monitoring in participants home-environment.

Study groups in NCT04079894
Study groupRoleWhat they receive
LSS ParticipantsPatients with lumbar spinal stenosis
Receives: Other: Standard Movement Protocol; Device: Accerelerometer Monitoring
Background populationPopulationdata from existing research project
Receives: Device: Accerelerometer Monitoring
LBP ParticipantsPatients with Low back Pain
Receives: Device: Accerelerometer Monitoring

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Accelerometer-data

    Raw accelerometer data will be collected by four accelerometers (Axivity AX3. ), which will be placed at the participants' hip in the midaxillary line, at the thigh, ankle and on the lower back, secured by hypo-allergenic band aids.

    Measured: Collected during the Standardized Movement Protocol at baseline.

  2. Accelerometer-data

    Raw accelerometer data collected for 7 consecutive days, by one accelerometer (Axivity AX3) secured by band-aid. The placement of the accelerometer will be decided in phase A.

    Measured: At baseline

  3. Accelerometer-data

    Raw accelerometer data collected for 7 consecutive days, by one accelerometer (Axivity AX3) secured by band-aid. The placement of the accelerometer will be decided in phase A.

    Measured: 3 months post-surgery

  4. The Self-Paced Walking Test

    Walking on a pre-determined rute until stopped by symptoms of LSS. Recording time and distance walked.

    Measured: At baseline as part of the Standardized Movement Procotol

  5. The Self-Paced Walking Test

    Walking on a pre-determined rute until stopped by symptoms of LSS. Recording time and distance walked.

    Measured: At baseline

  6. The Self-Paced Walking Test

    Walking on a pre-determined rute until stopped by symptoms of LSS. Recording time and distance walked.

    Measured: 3 months post-surgery

  7. The Oswestry Disability Index

    Questionnaire on function in patients with lower back pain. Score 0-100% where 100% is severe disability

    Measured: At baseline

  8. The Oswestry Disability Index

    Questionnaire on function in patients with lower back pain. Score 0-100% where 100% is severe disability

    Measured: 3 months post-surgery.

Secondary outcomes (10)
  1. The Swiss Spinal Stenosis Questionnaire

    Questionnaire on function in patients with spinal stenosis. Score 0-100% where 100% indicates severe disability.

    Measured: At baseline

  2. The Swiss Spinal Stenosis Questionnaire

    Questionnaire on function in patients with spinal stenosis. Score 0-100% where 100% indicates severe disability.

    Measured: 3 months post-surgery

  3. Visual Analog Scale for Back and Leg Pain

    Scale from 0-100. 100 indicating worse pain ever experienced.

    Measured: At baseline

  4. Visual Analog Scale for Back and Leg Pain

    Scale from 0-100. 100 indicating worse pain ever experienced.

    Measured: 3 months post-surgery

  5. Hospital Anxiety and Depression Scale

    Questionnaire on anxiety and depression. Rating anxiety and depression seperately on an ordinal scale from 0-21, 21 indicating worst result.

    Measured: At baseline

  6. Hospital Anxiety and Depression Scale. Rating anxiety and depression seperately on an ordinal scale from 0-21, 21 indicating worst result.

    Questionnaire on anxiety and depression

    Measured: 3 months post-surgery

  7. Mean Change from Baseline in Accelerometer Measures at 3 Months Post-Surgery

    Axivity AX3 secured by band-aids

    Measured: 3-months post-surgery

  8. Mean Change from Baseline in The Self-Paced Walking Test at 3 Months Post-Surgery

    Walking on a pre-determined rute until stopped by symptoms of LSS. Recording time and distance walked.

    Measured: 3 months post-surgery

  9. Mean Change from Baseline in The Oswestry Disability Index at 3 months Post-Surgery

    Questionnaire on function in patients with lower back pain

    Measured: 3 months post-surgery

  10. Mean Change from Baseline in The Swiss Spinal Stenosis Questionnaire at 3 Months Post-Surgery

    Questionnaire on function in patients with spinal stenosis

    Measured: 3 months post-surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Sep 2019
  2. Study start26 Jun 2019
  3. Primary completion1 Feb 2023
  4. Study completion1 Feb 2023

Resources

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
Prospective
Enrolment
206 participants (actual)
Target duration
3 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT04079894
Sponsor's protocol ID
OP_884
Other IDs
20182000-128, OP_884
Acronym
PAESP
Status last verified
Mar 2023
First submitted
5 Jun 2019
Last updated
16 Mar 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All IPD that underlie results of scientific articles

Publications

  • Lurie J, Tomkins-Lane C. Management of lumbar spinal stenosis. BMJ. 2016 Jan 4;352:h6234. doi: 10.1136/bmj.h6234.

    PubMed 26727925
  • Ammendolia C, Stuber K, Tomkins-Lane C, Schneider M, Rampersaud YR, Furlan AD, Kennedy CA. What interventions improve walking ability in neurogenic claudication with lumbar spinal stenosis? A systematic review. Eur Spine J. 2014 Jun;23(6):1282-301. doi: 10.1007/s00586-014-3262-6. Epub 2014 Mar 15.

    PubMed 24633719
  • Norden J, Smuck M, Sinha A, Hu R, Tomkins-Lane C. Objective measurement of free-living physical activity (performance) in lumbar spinal stenosis: are physical activity guidelines being met? Spine J. 2017 Jan;17(1):26-33. doi: 10.1016/j.spinee.2016.10.016. Epub 2016 Oct 25.

    PubMed 27793759
  • Henrica C. W. de Vet CBT, Lidwine B. Mokkink, Dirk L. Knol (2011) Measurement in Medicine A Practical Guide

  • Jespersen AB, Gustafsson MEAK. Correlation between the Oswestry Disability Index and objective measurements of walking capacity and performance in patients with lumbar spinal stenosis: a systematic literature review. Eur Spine J. 2018 Jul;27(7):1604-1613. doi: 10.1007/s00586-018-5520-5. Epub 2018 Mar 5.

    PubMed 29508075
  • Tomkins CC, Battie MC, Rogers T, Jiang H, Petersen S. A criterion measure of walking capacity in lumbar spinal stenosis and its comparison with a treadmill protocol. Spine (Phila Pa 1976). 2009 Oct 15;34(22):2444-9. doi: 10.1097/BRS.0b013e3181b03fc8.

    PubMed 19829259
  • Webber SC, St John PD. Comparison of ActiGraph GT3X+ and StepWatch Step Count Accuracy in Geriatric Rehabilitation Patients. J Aging Phys Act. 2016 Jul;24(3):451-8. doi: 10.1123/japa.2015-0234. Epub 2016 Jan 11.

    PubMed 26751505
  • Treacy D, Hassett L, Schurr K, Chagpar S, Paul SS, Sherrington C. Validity of Different Activity Monitors to Count Steps in an Inpatient Rehabilitation Setting. Phys Ther. 2017 May 1;97(5):581-588. doi: 10.1093/ptj/pzx010.

    PubMed 28339904
  • McCullagh R, Dillon C, O'Connell AM, Horgan NF, Timmons S. Step-Count Accuracy of 3 Motion Sensors for Older and Frail Medical Inpatients. Arch Phys Med Rehabil. 2017 Feb;98(2):295-302. doi: 10.1016/j.apmr.2016.08.476. Epub 2016 Sep 22.

    PubMed 27666157
  • Dijkstra B, Kamsma Y, Zijlstra W. Detection of gait and postures using a miniaturised triaxial accelerometer-based system: accuracy in community-dwelling older adults. Age Ageing. 2010 Mar;39(2):259-62. doi: 10.1093/ageing/afp249. Epub 2010 Jan 18. No abstract available.

    PubMed 20083616
  • Park J, Ishikawa-Takata K, Tanaka S, Bessyo K, Tanaka S, Kimura T. Accuracy of Estimating Step Counts and Intensity Using Accelerometers in Older People With or Without Assistive Devices. J Aging Phys Act. 2017 Jan;25(1):41-50. doi: 10.1123/japa.2015-0201. Epub 2016 Aug 24.

    PubMed 27180730

Questions about this trial

What is this clinical trial studying?

An observational study of Lumbar Spinal Stenosis and Low Back Pain, run by Malin Eleonora av Kák Gustafsson, MD at 1 site in Denmark.

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 5 inclusion and 10 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 16 Mar 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 Denmark. 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?

Accelerometer-data (time frame: Collected during the Standardized Movement Protocol at 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?

On the ClinicalTrials.gov record for NCT04079894, which also lists 11 linked publications.

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 16 Mar 2023; AzTrials last refreshed its copy on 27 Oct 2026.

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