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Ankylosing SpondylitisNCT07891507

Nurse-Led Exercise Program for Older Adults With Ankylosing Spondylitis

A study testing Nurse-Led Tailored Exercise Program in people with Ankylosing Spondylitis, run by Mansoura University at 1 site in Egypt.

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

This study evaluated whether a nurse-led tailored exercise program improves spinal mobility, functional ability, pain, and health literacy in adults aged 60 years or older with ankylosing spondylitis. Read more about this study

Who is it for?
Ages 60 years and older
Conditions the study is for
Ankylosing Spondylitis
What is being tested?
Nurse-Led Tailored Exercise Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteEgypt
Study dates
1 Nov 2025to 1 May 2026
Phase
Interventional

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
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged 60 years or older
  • Diagnosis of ankylosing spondylitis for at least 2 years, established by the treating rheumatologist and documented in the medical record
  • Currently receiving treatment
  • Alert and able to communicate
  • Willing to participate

Who cannot join

  • Other rheumatologic diseases
  • Dementia or other cognitive impairment affecting communication or consent
  • Uncorrected visual or hearing impairment

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Sohag University Hospital, Rheumatology and Rehabilitation Outpatient Clinics

    Sohag, Sohag Governorate, 82524

Other trials in Egypt

About this study

Official title: Effects of a Nurse-Led Tailored Exercise Program on Spinal Mobility, Functional Ability, Pain, and Health Literacy Among Older Adults With Ankylosing Spondylitis: A Quasi-Experimental Study

This study evaluated whether a nurse-led tailored exercise program improves spinal mobility, functional ability, pain, and health literacy in adults aged 60 years or older with ankylosing spondylitis. Participants received five individual sessions over 2 weeks covering disease education, neck, shoulder, back, trunk, pelvic, lower-limb, and breathing exercises, and posture during daily activities, followed by home practice with telephone follow-up. Outcomes were assessed before the program and approximately 3 months after it.

Read the detailed description

Design: single-group pretest-posttest quasi-experimental study conducted in the outpatient Rheumatology and Rehabilitation clinics of Sohag University Hospital, Egypt. Fifty older adults with ankylosing spondylitis diagnosed by a rheumatologist for at least 2 years were enrolled. The intervention consisted of five individual sessions (10-35 minutes each, every 3-4 days over 2 weeks), an illustrated exercise booklet, a daily exercise log, home practice 5 days per week for 20-30 minutes, and twice-weekly telephone follow-up during the program. Exercises were progressed gradually and modified or stopped if pain, dizziness, or unusual shortness of breath occurred. Outcomes (BASMI, BASFI, pain VAS, and the Functional, Communicative, and Critical Health Literacy questionnaire) were measured at baseline and approximately 14 weeks after baseline. This study was registered retrospectively after completion.

Being tested
Nurse-Led Tailored Exercise Program
Keywords
Exercise Therapy; Older Adults; Nurse-Led Intervention; Health Literacy; Spinal Mobility; Physical Function
Medical subject headings
Spondylitis, Ankylosing

What participants receive

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

  • Nurse-Led Tailored Exercise ProgramBehavioural

    Five individual sessions over 2 weeks: (1) disease education and goal setting; (2) neck, arm, and shoulder exercises; (3) back, trunk, pelvic, lower-limb, and breathing exercises; (4) posture and body mechanics during daily activities; (5) consolidation and self-management. Home practice 5 days/week for 20-30 minutes using an illustrated booklet and exercise log, with twice-weekly telephone follow-up during the program.

Study groups in NCT07891507
Study groupRoleWhat they receive
Nurse-Led Tailored Exercise ProgramExperimentalOlder adults with ankylosing spondylitis received five individual nurse-led sessions over 2 weeks, followed by home exercise practice with telephone follow-up.
Receives: Behavioral: Nurse-Led Tailored Exercise Program

What is being measured

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

  1. Change in Spinal Mobility (Bath Ankylosing Spondylitis Metrology Index, BASMI)

    Clinician-measured composite of five mobility measurements; score 0-10, higher scores indicate greater impairment.

    Measured: Baseline and approximately 14 weeks after baseline (3 months after program completion)

  2. Change in Functional Ability (Bath Ankylosing Spondylitis Functional Index, BASFI)

    Self-reported 10-item index; score 0-10, higher scores indicate worse function.

    Measured: Baseline and approximately 14 weeks after baseline (3 months after program completion)

Secondary outcomes (2)
  1. Change in Pain Intensity (Visual Analogue Scale)

    Spinal pain over the preceding week on a 0-10 scale; higher scores indicate more pain.

    Measured: Baseline and approximately 14 weeks after baseline (3 months after program completion)

  2. Change in Health Literacy (Functional, Communicative, and Critical Health Literacy Questionnaire)

    14 items; total score 0-28, higher scores indicate better health literacy.

    Measured: Baseline and approximately 14 weeks after baseline (3 months after program completion)

Timeline

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

  1. First posted23 Oct 2026
  2. Study start1 Nov 2025
  3. Primary completion1 Apr 2026
  4. Study completion1 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07891507
Sponsor's protocol ID
MANSOURA-NUR-AS-2025
Status last verified
Oct 2026
First submitted
17 Oct 2026
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data underlying the results reported in the publication (demographic and clinical characteristics, BASFI, BASMI, pain VAS, and FCC-HL scores at baseline and follow-up) will be shared with qualified researchers upon reasonable request.

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