NCT07238751

Brief Summary

The aim of this randomized controlled trial is to find the effects of Bowen technique with retro-walking on hamstring flexibility, pain, dynamic mobility and knee related disability in knee Osteoarthritis patients

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at below P25 for not_applicable knee-osteoarthritis

Timeline
4mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Oct 2025Sep 2026

First Submitted

Initial submission to the registry

September 25, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

October 25, 2025

Completed
26 days until next milestone

First Posted

Study publicly available on registry

November 20, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 20, 2026

Expected
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 25, 2026

Last Updated

November 20, 2025

Status Verified

November 1, 2025

Enrollment Period

11 months

First QC Date

September 25, 2025

Last Update Submit

November 18, 2025

Conditions

Keywords

Knee OsteoarthritisHamstring tightnessBowen techniqueRetro-walking

Outcome Measures

Primary Outcomes (5)

  • Visual Analogue scale VAS

    The VAS is psychomotor response scales to investigate a unidimensional measure of pain intensity. It scores ranges from 0-10, 0 means No pain and 10 means Severe pain. Patient will be asked to verbally report the pain score.

    4 weeks

  • Active knee extension test

    Active knee extension will use to access the flexibility of the hamstring muscle. Ask the patient to lay down in spine position while flexing the hip 90-degree, other leg down with couch and leg to be test with both hands. The goniometer will place on knee and ask the patient to extend the knee holding hip flex 90 degree

    4 weeks

  • SLR

    A goniometer will be used to measure the range of hip flexion on passive SLR and range less than 80 degree indicate that the hamstring muscle tightness

    4 weeks

  • Timed Up and Go (TUG) Test

    The TUG test measures the time taken by a participant to stand up from a standard chair, walk a distance of 3 meters, turn around, walk back to the chair, and sit down. It assesses dynamic balance and functional performance.

    4 weeks

  • Knee injury and osteoarthritis score

    In KOOS include 42 items in five subscales to check different categories i.e. pain (9 items), symptoms (7 items), functions in the activity of daily living (ADLs) (17) items), sports and recreational activities (5 items), and quality of life (4 items).

    4 weeks

Study Arms (2)

Bowen technique with Retro-walking

OTHER

Bowen technique with Retro-walking

Other: Bowen technique with Retro-walking

Conventional PT

OTHER

Conventional PT

Other: Conventional Treatment

Interventions

In initially step the patient in prone position and therapist approach on the same side of the treatment limb. Use the thumb by applying the pressure on the lateral side of the target muscle. The treatment sequence will begin with thumb gradually involve the finger. a single treatment consists of a series of specific sequences of these moves with frequent pauses 2 to 5 minutes to allow time for the body to respond. Treatment session duration 15-20 minutes occur 3 days per week, for 4 weeks. Week 1(retro-walking on flat surface for 5 minutes) week 2(retro walking on flat surface for 7 minutes) week 3(retro-walking on flat surface for 10 minutes) week 4 (retro-walking on flat surface for 15 minutes) .Conventional PT including 1- hot pack 2-isometric quadriceps exercise(1 set of 10 reps twice a day)2-SLR stretch (1set of 10 reps twice a day)4-isometric hip adduction exercise( 1 set of 10 reps twice a day)5-Terminal knee extension( 1 set of 10 reps twice a day) total duration is 3 sessions

Bowen technique with Retro-walking

Conventional PT including 1-. Hot pack 2- isometric quadriceps exercise (1 set of 10 reps twice a day) 3-SLR Stretch (1set of 10 reps twice a day) 4 -isometric hip adduction exercise (1 set of 10 reps twice a day) 5-Terminal knee extension (1 set of 10 reps twice a day) Total duration is 3 sessions per week for 4 consecutive weeks.

Conventional PT

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age 40-60 years
  • Both gender: male and female
  • Less than 80-degree hip flexion angle on passive SLR, Active knee extension greater than 20 indicates hamstring muscle tightness
  • Kellgren and Lawrence classification (stage I and stage II)
  • Bilateral hamstring tightness
  • Visual analogue scale value greater than 3
  • Pain duration more than 3 months

You may not qualify if:

  • Meniscal injury or ligamentous injury
  • Muscle/tendon injuries of hamstring
  • Spinal Injuries and any other co- morbidity
  • Any surgery, infection, trauma, pregnancy, fracture and fall
  • Involvement in regular flexibility yoga program
  • Patient with intra articular steroidal therapy with in last 6 months
  • Patient involvement in another intervention study
  • Malignancy
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shaafi international hospital,ISLAMABAD

Islamabad, Punjab Province, 46600, Pakistan

RECRUITING

MeSH Terms

Conditions

Osteoarthritis, Knee

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Officials

  • KINZA ANWAR, MS-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

KINZA ANWAR, MS-OMPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 25, 2025

First Posted

November 20, 2025

Study Start

October 25, 2025

Primary Completion (Estimated)

September 20, 2026

Study Completion (Estimated)

September 25, 2026

Last Updated

November 20, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations