Aerobic Versus Resistance Exercises on Disability After Abdominal Myomectomy
RE
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
This study will be conducted to compare aerobic and resistance exercises on disability after abdominal myomectomy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 16, 2026
CompletedFirst Posted
Study publicly available on registry
June 22, 2026
CompletedStudy Start
First participant enrolled
June 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 30, 2026
June 22, 2026
June 1, 2026
4 months
June 16, 2026
June 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
functional disability
Functional Independence Measure Scale was used to assess functional disability. it includes 18 items divided into two domains: Motor tasks (13 items) and cognitive tasks (5 items). score (1-7) to each of the 18 items based on the patient's observed performance.-Total FIM score range: 18 (complete dependence) to 126 (complete independence).
up to 12 weeks
pain intensity
Visual analogue scale consisted of a line, usually 100mm long, the patient was instructed to place a vertical mark on to indicate his pain, ranging from no pain or discomfort (0), to the worst pain (100) that the patient could feel
up to 12 weeks
Secondary Outcomes (1)
rectus abdominal muscle strength
up to 12 weeks
Study Arms (2)
aeropic exercises
EXPERIMENTALThirty patients who have undergone abdominal myomectomy will receive resisted exercises program for, 3 sessions per week for 12 weeks in addition to the routine medical treatment
Resistance Exercises
EXPERIMENTALthirty patients who have undergone abdominal myomectomy will receive aerobic exercises program for, 3 sessions per week for 12 weeks in addition to the routine medical treatment
Interventions
* Treadmill Walking: will begin at a low speed and incline, progressing gradually based on endurance. * Stationary Cycling: Low resistance cycling, will focus on steady, rhythmic pedaling. * Step Aerobics: Low-impact stepping movements to music, with a focus on maintaining proper posture. * The workload was increased incrementally by adjusting: Speed (walking/cycling pace), Resistance (stationary cycling or water exercises), Duration (gradually increasing from 20 to 30 minutes for the main session), Intensity progression was based on the Rate of Perceived Exertion (RPE) or patient-reported effort, ensuring safe advancement.
The patient will be prepared with preparatory explanations about each tool will be utilized i.e., sand bags, thera Bands, and swiss ball.Twelve exercises will be utilized for 12 weeks, three sessions/ week. The intervention will be applied by a trained physical therapist. First of all, each participant will be instructed to relax thighs, bottom and abdomen musculature.Each participant will be able to do 10 slow contractions each time, holding them for 10 seconds each with rests of 4 seconds in between. Then do not hold your breath or tighten rectus abdominis muscles at the same time. Will instruct participants to try holding each squeeze for a few seconds utilizing sand bags, thera band, and swiss balls.
Eligibility Criteria
You may qualify if:
- All patients are conscious and ambulant.
- Their ages ranged from 30-60 years old.
- All patients will be under post abdominal myomectomy (6-12 months) management program.
- All patients will not suffer from any complication post abdominal myomectomy, except weakness of abdominal muscles.
- All patients will receive and agreed to sign the informed consent form.
You may not qualify if:
- The patient who has cardiovascular diseases, or uncontrolled hypertension.
- The patient who has cardiac pacemakers or other implanted electronic devices.
- Uncooperative patients.
- Patients who have cardiopulmonary diseases.
- Patients who have psychic disorders.
- Patients with neuromuscular diseases.
- Pregnant female.
- Patients who have any endocrine, metabolic, renal or hepatic diseases. Patients who have an open wound at or near the treatment site.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : norhan khalaf awad ahmed
Study Record Dates
First Submitted
June 16, 2026
First Posted
June 22, 2026
Study Start
June 25, 2026
Primary Completion (Estimated)
October 30, 2026
Study Completion (Estimated)
October 30, 2026
Last Updated
June 22, 2026
Record last verified: 2026-06