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RecruitingNCT07929116Updated Nov 10, 2026

Gryrotonic Training in Behcet-diseased Elders With Breast Cancer

An interventional study of exercise in Breast Cancer and Behcet Disease, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to female participants aged 65 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

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

Updated Nov 10, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
65 Years to 75 Years
Sex
Female
01

Study summary

gryrotonic training may be a good exercise modality in Behcet-diseased elders with breast cancer

Read the detailed description

forty Behcet-diseased elders with breast cancer will randomy divide into group I (receive gyrotonic exercise three session weekly for 12 week) or group II (wait list)

02

Conditions studied

  • Breast Cancer
  • Behcet Disease
03

In context

Breast Neoplasms

14,825 studies on the registry are indexed under Breast Neoplasms; 3,319 are open to participants now.

This study's planned enrollment of 40 is below the median of 72 across 10,896 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 75 Years
Sexes eligible
Female
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

  • beast cancer survivors
  • behcet diseas patients

Exclusion criteria

Exclusion Criteria:

  • cardiac or repiratory or renal failure patients
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    group number 1

    twenty Behcet-diseased elders who survived from breast cancer will receive gyrotonic exercise three session weekly for 12 week. the session will 45 min

    Behavioral: exercise

  • No intervention
    group number 2

    twenty Behcet-diseased elders who survivied from breast cancer will be wait list for 12 weeks

Interventions

  • Behavioralexercise

    twnety Behcet-diseased elders who survived from breast cancer will receive gyrotonic exercise three session weekly for 12 week. the session will last for 45 min

06

What researchers measure

Primary outcomes

  1. Short Physical Performance Battery

    the total score will be calcualted

    Time frame: it will be measured after 12 weeks

Secondary outcomes

  1. Dual task gait speed

    this task assess gait speed

    Time frame: It will be measured after 12 weeks

  2. Four-square step test

    it is fucntional balnce test

    Time frame: It will be measured after 12 weeks

  3. grip strenghts

    it is a measure of grip strenghths in dominant hand

    Time frame: It will be measured after 12 weeks

  4. time up- and go testing

    it is a measure of fall risk

    Time frame: It will be measured after 12 weeks

  5. sit-to-stand 30-second testing

    asess number of repteations of sit-to-staning in 30 seconds

    Time frame: It will be measured after 12 weeks

  6. six minute walking testingg

    distance covered by subject in six minutes wil be assessed

    Time frame: It will be measured after 12 weeks

  7. 10-meters walking testing

    time covered for walking for ten meter will be assessed

    Time frame: It will be measured after 12 weeks

  8. trunk-flexor McGill core endurance test

    this test will assess endurance of trunk flexors

    Time frame: It will be measured after 12 weeks

  9. trunk-extensor McGill core endurance test

    this test will assess endurance of trunk extensors

    Time frame: It will be measured after 12 weeks

  10. right-lateral-trunk-bending McGill core endurance test

    this test will assess endurance of right lateral trunk bendors

    Time frame: It will be measured after 12 weeks

  11. left-lateral-trunk-bending McGill core endurance test

    this test will assess endurance of left lateral trunk bendors

    Time frame: It will be measured after 12 weeks

  12. arm flexion in thrity seconds

    it will assess numbers (repeations) of arm flexion in thirty second

    Time frame: It will be measured after 12 weeks

  13. maximal nubmer of push up

    this will assess maximal number of performed psh ups in speciifc time

    Time frame: It will be measured after 12 weeks

  14. behcet disease quality of life

    questioanire that will assess life quality in behcet disease (total score will be estiamted)

    Time frame: It will be measured after 12 weeks

  15. total score of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess quality of life

    Time frame: It will be measured after 12 weeks

  16. physical fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess physical fucntion related quality of life

    Time frame: It will be measured after 12 weeks

  17. role fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess role fucntion related quality of life

    Time frame: It will be measured after 12 weeks

  18. emotional fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess emotional fucntion related quality of life

    Time frame: It will be measured after 12 weeks

  19. cognitive fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess cognitive fucntion related quality of life

    Time frame: It will be measured after 12 weeks

  20. social fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess social fucntion related quality of life

    Time frame: It will be measured after 12 weeks

  21. fatigue fucntioning subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess fatigue

    Time frame: It will be measured after 12 weeks

  22. nausea-vomiting subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it is a questioaire asess nausea-vomiting

    Time frame: It will be measured after 12 weeks

  23. pain subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess pain

    Time frame: It will be measured after 12 weeks

  24. dyspnea subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess dyspnea

    Time frame: It will be measured after 12 weeks

  25. insomnia subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess insomnia

    Time frame: It will be measured after 12 weeks

  26. appetite-loss subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess appetite loss

    Time frame: It will be measured after 12 weeks

  27. constipation subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess constipation

    Time frame: It will be measured after 12 weeks

  28. diarrhea subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess diarrhea

    Time frame: It will be measured after 12 weeks

  29. financial difficulties subscale of European-Organization-for-Research and Treatment-of-Cancer Quality-of-Life Questionnaire-Core 30

    it will assess financial difficulties

    Time frame: It will be measured after 12 weeks

07

Study locations

1 of 1 sites recruiting
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07929116
Lead sponsor
Cairo University
Responsible party
Ali Mohamed Ali ismail (lecturer at cairo university faculty of phsyical therapy, Cairo University) — Principal investigator
First posted
Nov 10, 2026
Start date
Nov 30, 2026 (estimated)
Primary completion
May 30, 2027 (estimated)
Completion
May 30, 2027 (estimated)
Last update
Nov 10, 2026

Study contacts

Ali MA Ismail, PhD
Contact
ali.mohamed@pt.cu.edu.eg
+201005154209
fatma mohamed, PhD
Contact
fatma1995@gmail.com
01031321109
Ali MA Ismail, phd
principal investigator · Cairo University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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