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AzTrials

Parkinson DiseaseNCT07244900

Conventional Physical Therapy Action Observation Therapy on Freezing of Gait and Functional Mobility in Parkinson's Disease

A study testing Conventional Physical Therapy and Action Observation plus conventional Physical Therapy in people with Parkinson Disease and Neuro-Degenerative Disease, run by University of Lahore at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this study is to determine the effects of action observation therapy with conventional physical therapy on freezing gait and functional limitation in participants with Parkinson's disease. Read more about this study

Who is it for?
Ages 50 to 80 years
Conditions the study is for
Parkinson Disease, Neuro-Degenerative Disease
What is being tested?
Conventional Physical Therapy and Action Observation plus conventional Physical Therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
42 participants
Where
1 sitePakistan
Study dates
1 Jun 2023to 1 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • The exclusion criteria were
  • systemic diseases such as diabetes, sepsis, systemic lupus erythematosus
  • Uncontrolled hypertension or hypotension
  • 2. neurological issues that could affect the assessment and outcomes of treatment, 3. implantation for deep brain stimulation 4. visual or acoustic limitations.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • The University of Lahore

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Effects Of Conventional Physical Therapy With And Without Action Observation Therapy On Freezing Of Gait And Functional Mobility In Participants With Parkinson's Disease: A Randomised Clinical Trial

The goal of this study is to determine the effects of action observation therapy with conventional physical therapy on freezing gait and functional limitation in participants with Parkinson's disease.

Read the detailed description

Parkinson's disease is a neurodegenerative disorder that is characterized by rigidity, tremors, and bradykinesia, along with non-motor dysfunction. The exercise rehabilitation has a positive impact on motor and non-motor functions in individuals with Parkinson's disease. Conventional physical therapy (CPT) that involves isometric exercises, stretching techniques, and strength and balance training is useful to improve the severity of functional mobility and freezing of gait. In action observation therapy (AOT), small video clips of different goal-directed tasks were added to rehabilitation to determine the combined effects on outcome.

Being tested
Conventional Physical Therapy, Action Observation plus conventional Physical Therapy
Keywords
Parkinson's Disease, Balance, Freezing of Gait, Mobility, Function
Medical subject headings
Parkinson Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional Physical TherapyOther

    Group A received conventional physical therapy treatment. The CPT program consists of isometric exercises, stretching, and strength training based on the patient's physical condition and the severity of functional mobility and freezing of Gait.

  • Action Observation plus conventional Physical TherapyOther

    Group B was given action observation therapy with conventional physical therapy treatment. In AOT, the therapist showed small video clips of different goal-directed tasks to participants, and they were asked to follow every step and movement. The therapist maintained the patient's attention with verbal feedback

Study groups in NCT07244900
Study groupRoleWhat they receive
Conventional Physiotherapy GroupActive comparatorThis group included conventional physical therapy that contains isometric exercise, stretching techniques, and strength and balance training.
Receives: Other: Conventional Physical Therapy
Experimental GroupExperimentalThis group included action observation therapy in addition to conventional physical therapy, in which small videos containing specific task will be made available to follow to the participants.
Receives: Other: Action Observation plus conventional Physical Therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in functional mobility

    The TUG is an efficient test that measures mobility and balance, requiring participants to rise from a chair, walk 3 meters, turn, walk back, and sit down. The time taken to complete this sequence is recorded, with longer times indicating potential mobility issues. A score of more than or equal to fourteen seconds indicates a high risk of falls.

    Measured: The assessment was made at baseline before the treatment session, and any change in mobility status was observed at the end of 6th week and 12th week after the intervention.

  2. Change in Freezing of gait

    The FOG-Q is a reliable tool for evaluating the effectiveness of treatment intervention on FOG for Parkinson's disease. The questionnaire consists of 6 items designed to assess the severity of freezing of gait. Each item is rated on a five-point Likert scale, with '0' indicating no symptoms and '4' indicating the most severe symptoms. The total score can range from 0 to 24, with higher scores indicating greater severity of freezing of gait.

    Measured: The freezing of gait was assessed at baseline, and any change in it was measured at the end of 6th week and 12th week after the intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Nov 2025
  2. Study start1 Jun 2023
  3. Primary completion1 Jun 2024
  4. Study completion1 Jul 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study follows a parallel group design, involving two groups: a control group and an experimental group. Participants in both groups will receive treatment concurrently but under different conditions. The control group will receive the standard or conventional intervention, while the experimental group will receive the modified or additional treatment being investigated. Comparisons between the groups will be made to evaluate the effectiveness of the experimental intervention.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
42 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07244900
Sponsor's protocol ID
Kiran Maqsood
Status last verified
Nov 2025
First submitted
17 Nov 2025
Last updated
16 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data (IPD) that underlie the results reported in the study will be shared.

Questions about this trial

What is this clinical trial studying?

A study testing Conventional Physical Therapy and Action Observation plus conventional Physical Therapy in people with Parkinson Disease and Neuro-Degenerative Disease, run by University of Lahore at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in functional mobility (time frame: The assessment was made at baseline before the treatment session, and any change in mobility status was observed at the end of 6th week and 12th week after the intervention.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jun 2026; AzTrials last refreshed its copy on 7 Nov 2026.

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