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RecruitingNCT07929116ClinicalTrials.gov record

Gryrotonic Training in Behcet-diseased Elders With Breast Cancer

Breast Cancer · Behcet Disease

THE QUICK READ

What this study involves

The registry says this study is recruiting. Individual locations may have different availability.

Study type
Interventional
Phase
Not applicable
Age range
65 years - 75 years
Sex eligible
Female
Healthy volunteers
Not accepted
Participants
40 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

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

Read the full 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)

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

  • beast cancer survivors
  • behcet diseas patients

Exclusion Criteria:

  • cardiac or repiratory or renal failure patients
Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Random assignment
Masking
Single masked
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

group number 2

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

exercise BEHAVIORAL

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

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Short Physical Performance Battery

Time frame: it will be measured after 12 weeks

the total score will be calcualted

Secondary measures

Dual task gait speed

Time frame: It will be measured after 12 weeks

this task assess gait speed

Four-square step test

Time frame: It will be measured after 12 weeks

it is fucntional balnce test

grip strenghts

Time frame: It will be measured after 12 weeks

it is a measure of grip strenghths in dominant hand

time up- and go testing

Time frame: It will be measured after 12 weeks

it is a measure of fall risk

sit-to-stand 30-second testing

Time frame: It will be measured after 12 weeks

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

six minute walking testingg

Time frame: It will be measured after 12 weeks

distance covered by subject in six minutes wil be assessed

10-meters walking testing

Time frame: It will be measured after 12 weeks

time covered for walking for ten meter will be assessed

trunk-flexor McGill core endurance test

Time frame: It will be measured after 12 weeks

this test will assess endurance of trunk flexors

trunk-extensor McGill core endurance test

Time frame: It will be measured after 12 weeks

this test will assess endurance of trunk extensors

right-lateral-trunk-bending McGill core endurance test

Time frame: It will be measured after 12 weeks

this test will assess endurance of right lateral trunk bendors

left-lateral-trunk-bending McGill core endurance test

Time frame: It will be measured after 12 weeks

this test will assess endurance of left lateral trunk bendors

arm flexion in thrity seconds

Time frame: It will be measured after 12 weeks

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

maximal nubmer of push up

Time frame: It will be measured after 12 weeks

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

behcet disease quality of life

Time frame: It will be measured after 12 weeks

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

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess physical fucntion related quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess role fucntion related quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess emotional fucntion related quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess cognitive fucntion related quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess social fucntion related quality of life

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess fatigue

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

Time frame: It will be measured after 12 weeks

it is a questioaire asess nausea-vomiting

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

Time frame: It will be measured after 12 weeks

it will assess pain

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

Time frame: It will be measured after 12 weeks

it will assess dyspnea

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

Time frame: It will be measured after 12 weeks

it will assess insomnia

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

Time frame: It will be measured after 12 weeks

it will assess appetite loss

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

Time frame: It will be measured after 12 weeks

it will assess constipation

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

Time frame: It will be measured after 12 weeks

it will assess diarrhea

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

Time frame: It will be measured after 12 weeks

it will assess financial difficulties

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Cairo UniversityGiza, Dokki, EgyptRecruiting

Study team and timeline

Lead sponsor
Cairo University
Study start
Nov 30, 2026 Estimated
Primary completion
May 30, 2027 Estimated
Study completion
May 30, 2027 Estimated
First posted
Nov 10, 2026 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

Ali MA Ismail, PhDCONTACTali.mohamed@pt.cu.edu.eg+201005154209
fatma mohamed, PhDCONTACTfatma1995@gmail.com01031321109
Official study title

Gryrotonic Training in Behcet-diseased Elders With Breast Cancer

A HUMAN NEXT STEP

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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026