Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
Healthy Volunteers
NCT06921694

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

Led by University of Nottingham · Updated on 2025-12-12

88

Participants Needed

1

Research Sites

78 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-45 years
  • Willing and able to give informed consent
  • Suffering from chronic nonspecific low back pain lasting more than 3 months
  • Experiencing pain or functional limitations due to low back pain (minimum VAS score 3/10 or ODI score 5/50 or RMD score 5/24)
  • Able to exercise
Not Eligible

You will not qualify if you...

  • Radiating pain to leg, sciatica, or acute radiculopathy
  • Specific diagnosed spinal conditions such as herniated disk, degenerative disk disease, spondylolysis, spinal stenosis, spinal tumour, or facet joint damage
  • History of osteoporosis, arthritis, scoliosis, or kyphosis
  • Current spinal infection, cancer, or any bone fracture
  • History of spinal or back surgery
  • Unable to participate in physical activity or exercise
  • Pregnant or breastfeeding
  • History of substance abuse
  • History of psychiatric illness currently treated with medication
  • History or current neurological conditions such as epilepsy
  • Lack of access to adapted equipment like phone, computer, or functioning WIFI
  • Unable to understand and communicate in English
  • Participation in another research study with invasive procedures or financial incentives in the last 3 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Nottingham, Queen's Medical Centre

Nottingham, Notts, United Kingdom, NG7 2UH

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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