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A Study Investigating an Exercise and Education Programme for Individuals With Ankylosing Spondylitis

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University College Dublin

Status and phase

Completed
Phase 3

Conditions

Spondylitis, Ankylosing

Treatments

Other: Exercise and Education

Study type

Interventional

Funder types

Other

Identifiers

NCT00764686
1/378/1173
SS/2008/83

Details and patient eligibility

About

Ankylosing Spondylitis(AS) is a chronic, inflammatory, rheumatic disease (Khan, 2002). AS is associated with increased work disability and use of healthcare resources (Ward et al, 2008). Evidence suggests that group exercise is the most effective form of physiotherapy management for individuals with Ankylosing Spondylitis (Dagfinrud et al, 2008). To date, no research has been published in relation to short, intensive group exercise programmes.

This study aims to investigate the effects of a five day exercise and education programme for individuals with Ankylosing Spondylitis. Effects of the programme on disease activity, function and spinal mobility will be measured using using validated quantitative measures; the overall value of the programme for patients will be explored by means of semi-structured interviews.

Full description

Patients with a diagnosis of Ankylosing Spondylitis are referred to the 5-day exercise and education programme by consultant rheumatologists at the Mater Misericordiae University Hospital. All patients referred to the programmes beginning 06/24/2008 and 08/25/2008 will be invited to participate.

Participants scoring 0-6 on the Bath Ankylosing Spondylitis Metrology Index are classified as low disease severity level and are allocated to Group 1; participants with a score of 6.1-10 are classified as higher disease severity and allocated to Group 2. Group 1 has two hydrotherapy classes, a gym-based exercise class and an education session daily. Group 2 has one hydrotherapy class, a gym-based exercise class and an education session daily. Exercise sessions are 1 hour in duration and are given by staff physiotherapists. Education sessions are 1 hour in duration and are given by senior members of the rheumatology multi-disciplinary team at the Mater Misericordiae University Hospital.

Outcome will be assessed upon entry to the study (pre-intervention), at 5 days (post-intervention) and at 4 weeks (follow-up). A semi structured interview will be carried out with each participant immediately post-intervention to explore the overall value of the group programme for participants.

Enrollment

18 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A diagnosis of Ankylosing Spondylitis according to the modified New York criteria

Exclusion criteria

  • Patients for whom hydrotherapy or land-exercise have been contra-indicated
  • Cognitive Impairment
  • Patients unwilling to give informed, written consent

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

18 participants in 2 patient groups

1
Experimental group
Description:
Low disease severity group
Treatment:
Other: Exercise and Education
Other: Exercise and Education
2
Experimental group
Description:
Higher disease severity group
Treatment:
Other: Exercise and Education
Other: Exercise and Education

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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