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Effect of Pelvic Control Exercises in Stroke

Effect of Pelvic and Trunk Control Exercises on Function Outcome of Affected Upper Extremity in Stroke Patients

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06067724
Enrollment
40
Registered
2023-10-05
Start date
2023-05-20
Completion date
2024-04-07
Last updated
2024-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Brief summary

The purpose of the study is to investigate the combined effect of pelvic and trunk control exercises on muscle performance of affected upper extremity in stroke patients.

Detailed description

The study conducted on forty stroke patients. They assessed by Biodex System 3 Pro Isokinetic, Modified Ashworth Scale(MAS), Fugel Meyer Assessment scale (FMAS), Box and block test and hand grip dynamometer. Patients divided into control group and study group. The control group treated by a traditional physical therapy program.The study group treated by the traditional physical therap program in addition to pelvic and trunk control exercises for 40 min.

Interventions

OTHERPelvic and trunk control exercises

Patients in this group will be treated by the traditional physical therapy program in addition to a 18 sessions of pelvic and trunk control exercises for 40 min included abdominal drawing in maneuver for contraction of transversus abdominis pelvic tilting exercises and pelvic stabilization exercises from different positions. Pelvic tilting exercises included; anterior, posterior, lateral pelvic tilting and pelvic rotation on a therapeutic ball. Pelvic stabilization exercises include bridging, half bridging, clamshell from supine and side lying, quadribed exercises, weight shifting on the affected limb from standing by forward and diagonal reach out, ball bridging and rhythmic stabilization exercises

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
45 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patient's age will range from 45 - 60 years. * Muscle tone grade will range from 1 to 1+ according to modified Ashworth scale. * Duration of illness will range from 6 to 18 months after stroke onset. * Ability of the patient to stand without assistive devices.

Exclusion criteria

* • Other neurological or musculoskeletal disorders that might affect pelvic alignment such as severe arthritis, knee surgery, total hip joint replacement, lower limb fractures, contractures of fixed deformity or leg length discrepancy. * Severe chronic back and/or knee pain that might affected standing posture. * Recurrent stroke * Shoulder or upper limb injury that might affect the recovery. * Perceptual or cognitive dysfunctions. * BMI \> 30

Design outcomes

Primary

MeasureTime frameDescription
Biodex System 3 Pro IsokineticSix weeks after the beginning of the interventionChanges in peak muscle torque of upper limb muscles from baseline to four weeks after the beginning of intervention

Secondary

MeasureTime frameDescription
Fugl-Meyer Assessment for upper extremitySix weeks after the beginning of the interventionChanges in upper limb function from baseline to four weeks after the beginning of intervention
Box and block testSix weeks after the beginning of the interventionChanges in gross hand function from baseline to four weeks after the beginning of intervention
Hand grip dynamometerSix weeks after the beginning of the intervention. Changes in hand grip strength from baseline to four weeks after the beginning of intervention

Countries

Egypt

Contacts

Primary ContactRowida Abdelgleel, Assistant lecturer
rowidaabdelglel@gmail.com01152322678
Backup ContactNahed Salem, Professor
nahedsalem960@gmail.com+201224297063

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026