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Effects of Hip Focused Exercises in Patients With Post Operative Anterior Cruciate Ligament Rehabilitation

R

Riphah International University

Status

Completed

Conditions

Post Operative Anterior Cruciate Ligament Rehabilitation

Treatments

Other: Standard rehabilitation
Other: Hip focused

Study type

Interventional

Funder types

Other

Identifiers

NCT06750198
REC/RCR & AHS/24/0109

Details and patient eligibility

About

A Randomized Controlled Trial will be conducted at Mahaban Medical and Research Hospital through consecutive sampling technique on 66 patients which will be allocated using simple random sampling through sealed opaque enveloped into Group A and Group B. Group A will be treated with hip focused exercises and standard rehabilitation protocol while Group B will be treated with traditional exercises at the frequency of 2 sets with 10 repetitions and thrice a week. Outcome measures will be conducted through pain, range of motion, functional disability, muscle strength and endurance after 12 weeks. Data will be analyzed during SPSS software version 21. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non- parametric test will be used within a group or between two groups.

Full description

Anterior cruciate ligament plays an important role in knee stability and is prone to contact and and non-contact injuries. ACL reconstruction followed by proper rehabilitation is the most successful procedure to restore knee stability and ROM. Keeping in mind the lower limb kinematics and biomechanics the aim of this study will be to see the effects of hip focused exercises on pain, range of motion, functional disability, muscle strength and endurance in patients with post-operative ACL rehabilitation. A Randomized Controlled Trial will be conducted at Mahaban Medical and Research Hospital through consecutive sampling technique on 66 patients which will be allocated using simple random sampling through sealed opaque enveloped into Group A and Group B. Group A will be treated with hip focused exercises and standard rehabilitation protocol while Group B will be treated with traditional exercises at the frequency of 2 sets with 10 repetitions and thrice a week. Outcome measures will be conducted through pain, range of motion, functional disability, muscle strength and endurance after 12 weeks. Data will be analyzed during SPSS software version 21. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non- parametric test will be used within a group or between two groups.

Enrollment

47 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Both males and females of age group between 18 and 45 years

  • Patients with ACL reconstruction in early rehabilitation phase.
  • Physically or recreationally active a minimum of three times per week.(26)
  • 1-5 day post operatively(26)
  • Physically healthy and without patients with other medical history or joint deformities
  • Patients without severe meniscus or cartilage damage (27)
  • Complaints of pain (NPRS 3-7) and swelling in the operated knee

Exclusion criteria

Patients with multiple ligament injuries in the knee joint

  • Patients with knee osteoarthritis
  • Patients with joint infection (27)
  • An associated chondral defect requiring surgical intervention
  • A meniscus tear requiring a repair.
  • Patients with incomplete follow-up (28)
  • Presence of unstable medical conditions preventing the patient from participating in the rehabilitation program.
  • History of ipsi-lateral hip replacement
  • Ipsi-lateral hip osteoarthritis or lateral hip pain
  • Neurological or any other conditions affecting strength or function of lower limbs.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

47 participants in 2 patient groups

Hip focused exercises
Experimental group
Description:
will receive hip focused exercises and standard rehabilitation protocol with the frequency of 2 sets and 10 repetitions thrice per week for a total of 12 weeks. Pre and post intervention values will be taken on 1st day and after 12 weeks.
Treatment:
Other: Standard rehabilitation
Other: Hip focused
Standerd rehab protocol
Active Comparator group
Description:
will receive only standard rehabilitation protocol with the frequency of 2 sets and 10 repetitions thrice per week for a total of 12 weeks. Pre and post intervention values will be taken on 1st day and after 12 weeks
Treatment:
Other: Standard rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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