ClinicalTrials.Veeva

Menu

Effects of Orofacial Myofunctional Therapy on Mental Functioning and Overall Self-Sufficiency in Stroke Patients

U

University of Lahore

Status

Unknown

Conditions

Stroke

Treatments

Other: Routine physical therapy along with orofacial therapy
Other: Routine physical therapy treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT05061043
IRB-UOL-FAHS/892/2021

Details and patient eligibility

About

This project will explore the effects of orofacial myofunctional therapy on mental functioning and overall self-sufficiency in stroke patients. The population sample will be 70 divided randomly into two groups by concealed envelop method. Then i will collect data from Physiotherapy department Wapda Hospital complex, Lahore. Group A will be treated with routine physical therapy treatment that will include EMS, Infrared and Intermittent stretching of facial muscles for 36 sessions on alternate days, each session comprise 30 minutes . Group B will receive routine physical therapy along with orofacial therapy (36 sessions on alternate days, each session comprise 45 minutes) .

Full description

This project will explore the effects of orofacial myofunctional therapy on mental functioning and overall self-sufficiency in stroke patients. The population sample will be 70 divided randomly into two groups by concealed envelop method. Then i will collect data from Physiotherapy department Wapda Hospital complex, Lahore. Group A will be treated with routine physical therapy treatment that will include EMS, Infrared and Intermittent stretching of facial muscles for 36 sessions on alternate days, each session comprise 30 minutes . Group B will receive routine physical therapy along with orofacial therapy (36 sessions on alternate days, each session comprise 45 minutes) .According to the treatment protocol, the patients participated of the OMT sessions, lasting 45 minutes each, with a weekly frequency during the first 30 days and every two weeks after this period, with no other additional therapeutic conducts5 (treatment duration = 120 days). A home exercise program was pre- scribed during each session. 10 personal activities: feeding, personal toileting, bathing, dressing and undressing, getting on and off a toilet, controlling bladder, controlling bowel, moving from wheelchair to bed and returning, walking on level surface (or propelling a wheelchair if unable to walk) and ascending and descending stairs.

Enrollment

70 estimated patients

Sex

All

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Both Gender
  • Age (Years) 40-70
  • Subacute stage of a strok

Exclusion criteria

  • Trauma (e.g., temporal bone fracture)
  • Infection
  • Herpes zoster (Ramsay Hunt syndrome)
  • Borreliosis (Lyme disease)
  • HSV reactivation
  • HIV
  • Tumors (esp. parotid gland tumors)
  • Pregnancy
  • Diabetes mellitus
  • Guillain-Barré syndrome
  • Sarcoidosis
  • Amyloidosis
  • Stroke

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

Group A
Active Comparator group
Description:
Routine physical therapy treatment
Treatment:
Other: Routine physical therapy treatment
Group B:
Experimental group
Description:
Routine physical therapy along with orofacial therapy
Treatment:
Other: Routine physical therapy along with orofacial therapy

Trial contacts and locations

1

Loading...

Central trial contact

Janat zarar; MANAHIL ZARAR, MS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems