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NCT06921694Recruiting

A Combined Exercise Programme Involving Strengthening, Flexibility and Aerobic Exercise for Lower Back Pain

A Combined Exercise Programme Involving Strengthening, Flexibility and Aerobic Exercise for Lower Back Pain: a Randomised-controlled Study

Source: ClinicalTrials.gov · Last updated 12 Dec 2025

Brief summary (registry, in English)

This randomised controlled trial will evaluate the effectiveness of different exercise modalities for individuals with low back pain. Participants will be allocated to one of three groups: a control arm (usual exercise), a running-based intervention, or a swimming/cycling-based intervention. Outcomes related to pain and function will be measured at baseline, 8 weeks, and 12 months.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
88 (estimated)
First submitted
26 Mar 2025
Start date
1 Apr 2025
Primary completion date
30 Sept 2026
Lead sponsor
University of Nottingham
NCT number
NCT06921694

What you commit to

  • Study type: Interventional
  • Planned participants: 88
  • From 1 Apr 2025 to the primary completion date, 30 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of psychiatric illness (eg. depression, dementia, schizophrenia) for which currently taking medication

Other illness

  • Specific diagnosis/condition for LBP (e.g. herniated disk, degenerative disk disease, spondylolysis, spinal stenosis, spinal tumour, facet joint damage)
  • History of osteoporosis , arthritis, scoliosis, or kyphosis.
  • Current spinal infection, cancer or a current fracture (any bone).
  • History of spinal/back surgery
  • History of substance abuse
  • History or current neurological condition (e.g. epilepsy)

Other

  • Radiating pain to leg / sciatica / acute radiculopathy
  • Unable to participate in physical activity and exercise
  • Pregnant or breast feeding
  • Not in possession or have access to adapted equipment (phone, computer, functioning WIFI)
  • Unable to understand and communicate in English
  • Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance

Who the study is looking for

  • Aged 18-45 years
  • Participant is willing and able to give informed consent for participation in the study
  • Suffering from chronic NSLBP (more than 3 months, localised below the costal margin and above the gluteal folds)
  • Suffers from pain or functional limitations as a result of their LBP (minimum VAS (back) score of 3/10 or ODI score of at least 5/50 or RMD score of at least 5/24 (note, unlike ODI, RMD does not describe specific cuts offs for different levels of disability)
  • Able to exercise

Age in the registry: 18 years to 45 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Nottingham, Queen's Medical Centre
Coordinator of this site? Confirm its status
NottinghamUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.