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RecruitingNCT07894133Updated Oct 26, 2026

Gait Parameters in Breast Cancer Receiving Chemotherapy Patients

An observational study in Breast Cancer, Chemotherapy and Biodex Gait Trainer, sponsored by Adly A Adam. Recruiting at 1 site in Egypt. Open to female participants aged 40 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by Adly A Adam · Observational

From the registry’s dates

  • Started Oct 2026; still recruiting 1 month later.
Updated Oct 26, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
360
Ages
40 Years to 50 Years
Sex
Female
01

Study summary

Breast cancer is considered the most common type of malignancies, it is the most frequently diagnosed representing around 2.3 million cases. Where, their chemotherapy may cause fatigue affecting the overall quality of patient's life. Gait and balance are fundamental for activities of daily living and maintaining functional independence.

Read the detailed description

Gait disturbance is one of the side effects that occur after chemotherapy due to various reasons resulting in lower values of quality of life. Chemotherapeutic agents can cause muscle wasting particularly in the lower extremities resulting in reduced strength and balance. Gait dysfunction, and falls may have particularly severe consequences in this population due to comorbidities increasing the risk of fall-related injury. Therefore, this study was designed to assess gait parameters in breast cancer patient receiving chemotherapy to assist in designing on optimal rehabilitation program based on objective data derived from our study for gait dysfunction in breast cancer patients receiving chemotherapy.

02

Conditions studied

  • Breast Cancer
  • Chemotherapy
  • Biodex Gait Trainer
  • Gait Parameters

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Keywords

  • Chemotherapy
  • Breast cancer
  • Biodex gait trainer
  • Gait Parameters
  • National Cancer Institute
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 360 is above the median of 184 across 3,235 observational studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Adly A Adam is the lead sponsor of 12 studies on the registry; 6 are open to participants now.

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

04

Who can participate

Ages eligible
40 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

360 female patients aged from 40 to 50 years, suffering from breast cancer and receiving chemotherapy will be randomly selected from National Cancer Institute, Cairo, Egypt

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

  • Age ranged from 40 to 50 years old.
  • Female patients.
  • Suffering from breast cancer, and receiving chemotherapy.
  • Will be assessed before chemotherapy, 3 months and 6 months after chemotherapy.
  • All enrolled patients will have signed their signed.

Exclusion criteria

Exclusion Criteria:

  • No history of prior chemotherapy.
  • Current .
  • Orthopedic problems that affect balance and gait.
  • Diabetic patients with neuritis.
  • Peripheral neuropathy.
  • Polyarthritis.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
360 participants (estimated)
Target follow-up
3 Months
Patient registry
Yes

Groups and cohorts

  • Experimental Group

    360 female patients aged from 40 to 50 years, suffering from breast cancer and receiving chemotherapy

    Other: Gait parameter assessment

Interventions

  • OtherGait parameter assessment

    A Biodex Gait Trainer 3 (BIODEX MEDICAL SYSTEMS, INC., New York, NY, model NO. 601-1-M90, EN 60601- 1 USA), is a device which is used to assess the spatiotemporal gait parameters of patients . It consists of a treadmill with an instrumented deck that monitors and records kinematic gait parameters including gait speed, step cycle, step length, and time on each foot (step symmetry). The patient will instructed to stand on the treadmill holding on handrails to ensure safety. Each patient will be asked to walk continuously for 3 minutes, till the evaluation session ended, and the gait trainer slow down gradually until it stopped. Three successive trials will be done for each patient. The mean value of each variable of spatiotemporal parameters of gait \[walking speed (meters per seconds), step cycle (cycle per second), step length (meter), and time on each foot (seconds)\] will be recorded.

06

What researchers measure

Primary outcomes

  1. Walking Speed (Meter per second)

    Walking Speed in unit of measurement is meter per second.

    Time frame: One time assessment throughout the study completion an average of 3 months.

  2. Step cycle (cycle per second)

    Step cycle: in unit of measurement is Cycle per second.

    Time frame: One time assessment throughout the study completion an average of 3 months.

  3. Step length (Meter)

    Step length in unit of measurement is meter.

    Time frame: One time assessment throughout the study completion an average of 3 months.

  4. Time on each foot (Seconds)

    Time on each foot in unit of measurement is seconds

    Time frame: One time assessment throughout the study completion an average of 3 months.

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
Oct 26, 2026
Show all 1 update
  1. Oct 26, 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
NCT07894133
Lead sponsor
Adly A Adam
Responsible party
Adly A Adam (Physical Therapy Specialist, Cairo University) — Sponsor-investigator
First posted
Oct 26, 2026
Start date
Oct 1, 2026
Primary completion
Dec 1, 2026 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
Oct 26, 2026

Study contacts

Mustafa A Abdelhalim, B.Sc
Contact
adampt80a@gmail.com
01273902755 ext. 101
Noha MK Ahmed, PHD
Contact
adampt80a@gmail.com
01273902755 ext. 010
Wessam R ElGhamry, Assistant Professor
study chair · Assistant Professor of Clinical Oncology
Nesseren A Affiffy, Professor
study director · Professor of Physical Therapy for Surgery
Mostafa A Abdelhalim, B.Sc
principal investigator · Physical Therapist

Oversight

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

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