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Not yet recruitingNCT07761767Updated Aug 13, 2026

Self-Care Education for Joint Stiffness and Functional Ability in Rheumatoid Arthritis

An interventional study of self care educational program for the study group and Routine care in Rheumatoid Arthritis (RA), sponsored by Assiut University. Not yet recruiting. Open to participants aged 20 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-08-13.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
20 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 49 studies in Arthritis, Rheumatoid by Assiut University — 23 open to participants now, 23 under way, none of them phase 3. Arthritis, Rheumatoid · Assiut University.

Started
2026
with 9 others
No phase
5 of 49
1 open now
Primary completion
2027-01
later than 12 of 22 live
Registered
42nd of 49
by date

Among the 49 studies in Arthritis, Rheumatoid by Assiut University, this one is one of 10 that started in 2026, is one of 5 with no phase, reaches primary completion later than 12 of the 22 other live ones, and was the 42nd registered.

By phase

49 studies; the count open now beside each. This study's row is marked.

Observational43 · 22 open
No phasethis study5 · 1 open
Phase 41 · 0 open

By the year they started

First in 2016; this study’s year is marked. 10 started in 2026.

What they test

Size and results

Median enrollment 90 across the 6 interventional studies, 80 across the 43 observational. Of the 10 that completed or were terminated, 0 (0%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 49 studies in Arthritis, Rheumatoid by Assiut University, or all of them as a file.
02

Study summary

Rheumatoid arthritis is a chronic inflammatory autoimmune disease that may cause joint stiffness, pain, reduced mobility, and impaired functional ability. Self-care education may help patients improve their knowledge and practices related to disease management, joint protection, physical activity, exercise, energy conservation, and symptom management.

This study aims to evaluate the effectiveness of a self-care educational program on joint stiffness and functional ability among patients with rheumatoid arthritis. Participants will be assigned to either a study group or a control group. The study group will receive the self-care educational program in addition to routine care, while the control group will receive routine care only. Joint stiffness and functional ability will be assessed before and after implementation of the educational program.

Read the detailed description

Rheumatoid arthritis is associated with joint inflammation, stiffness, pain, reduced physical functioning, and limitations in activities of daily living. Appropriate self-care practices may contribute to improving patients' ability to manage symptoms and maintain functional independence.

The self-care educational program will provide patients with information and practical guidance regarding rheumatoid arthritis and its management. The program may include disease-related knowledge, medication adherence, joint protection techniques, exercise, energy conservation, activity modification, symptom management, and appropriate self-care practices.

Participants will be divided into two groups:

Study Group: Participants will receive the self-care educational program in addition to routine care.

Control Group: Participants will receive routine care only. Joint stiffness and functional ability will be assessed at baseline and after implementation of the educational program. The outcomes of the study group will be compared with those of the control group to determine the effectiveness of the program.

03

Conditions studied

  • Rheumatoid Arthritis (RA)

Keywords

  • Rheumatoid Arthritis
  • Self-Care
  • Joint Stiffness
  • Functional Ability
04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • The criteria for selection were: patients" age ranged between 20-65 years old; did not have any auditory, visual or psychological problems. Patients who are able to communicate and participate in the educational program.

Patients who agree to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Patients with severe cognitive or communication impairment. Patients with other severe musculoskeletal conditions that may affect functional ability.

Patients who have participated in a similar self-care educational program recently.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
110 participants (estimated)

Study arms

  • Experimental
    Self-Care Education Group

    Participants in the intervention group will receive a self-care educational program designed to improve self-care practices, reduce joint stiffness, and improve functional ability in patients with rheumatoid arthritis. The program will include education about rheumatoid arthritis, joint protection techniques, appropriate exercises, medication use, and self-care practices.

    Behavioral: self care educational program for the study group

  • Other
    Routine Care Group

    Participants will receive usual care without the self-care educational program.

    Other: Routine care

Interventions

  • Behavioralself care educational program for the study group

    study group Participants will receive the self-care educational program in addition to usual care.

  • OtherRoutine care

    The control group will receive the routine care provided to patients with rheumatoid arthritis and will not receive the self-care educational program during the study period.

06

What researchers measure

Primary outcomes

  1. change in joint stiffness

    Duration of morning joint stiffness will be assessed using a single-item patient-reported outcome measure. Participants will report the duration of their morning joint stiffness in minutes. Durations greater than 12 hours (720 minutes) will be recorded as 720 minutes. Higher values indicate a longer duration of morning joint stiffness. Severity of morning joint stiffness will be assessed using a single-item patient-reported outcome measure. Participants will rate the overall severity of their morning joint stiffness on a numerical rating scale ranging from 0 to 10, where 0 indicates no joint stiffness and 10 indicates the worst possible joint stiffness. Higher scores indicate greater severity of joint stiffness.

    Time frame: Baseline and 3 months after completion of the intervention.

Secondary outcomes

  1. functional ability

    Functional ability will be assessed using the Health Assessment Questionnaire-Disability Index (HAQ-DI). The HAQ-DI assesses functional ability across eight areas: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and activities. Each item is scored from 0 (without any difficulty) to 3 (unable to do). The overall score ranges from 0 to 3, with 0 indicating no disability and 3 indicating severe disability. Higher scores indicate worse functional ability and greater disability.

    Time frame: Baseline and 3 months after completion of the intervention.

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Seyam, M. H., Boghdady, E. S. G., Abo El-Ata, A. B., & Mahdy, N. E. S. (2024). Knowledge, Practices and Self-Care Management Behaviors for Rheumatoid Arthritis Patients. Port Said Scientific Journal of Nursing, 11(3), 48-68.

Related links

Individual participant data

Plan to share: No — There are no plans to make individual participant data available to other researchers.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Jan 2027, 4 months later.

Of 292 non-industry interventional studies with no phase under Arthritis, Rheumatoid, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 39. This study's planned 4 months is below that.

Counting every sponsor, half of 348 studies reached it within 27 months; a quarter within 13 and three quarters within 47.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 8, 2026
First posted
Aug 12, 2026
StartEst.
Sep 1, 2026
Primary completionEst.
Jan 1, 2027
CompletionEst.
Apr 1, 2027
Last update
Aug 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07761767
Lead sponsor
Assiut University
Responsible party
Rezk Abdallah Mohammed Mahmoud (Assistant Lecturer, Assiut University) — Principal investigator
First posted
Aug 12, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Jan 1, 2027 (estimated)
Completion
Apr 1, 2027 (estimated)
Last update
Aug 13, 2026

Study contacts

REZK A Mohammed, MSc
Contact
RizkAbdullah@nursing.aswu.edu.eg
1122883312 20+

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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