AzTrials
AzTrials

Cardio Vascular DiseaseNCT07814846

Effect of Pre-operative Program in Open Heart Surgery

A study testing Multimedia preoperative progarm and Traditional preoperative program in people with Cardio Vascular Disease and Heart Surgery, run by Pajeemas Kittipanya-Ngam at 1 site in Thailand.

Completed

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

Official record
Search all trials

Trial summary

The goal of this clinical trial is to learn the effect of self prepare by multimedia program before going to heart surgery. The main questions it aim to answer is: Is preparing for heart surgery on your own or with a physical therapist the same? Researchers were compare the effects of preoperative physical therapy… Read more about this study

Who is it for?
Ages 18 to 70 years
What is being tested?
Multimedia preoperative progarm and Traditional preoperative program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 siteThailand
Study dates
17 Dec 2020to 31 Dec 2023
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 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients who undergoing elective open-heart surgery at the Queen Sirikit Heart Center of the Northeast, Faculty of Medicine, Khon Kaen University, Thailand
  • Age 18-70 years old
  • No lung atelectasis
  • No communication limit

Who cannot join

  • Lung diseases such as COPD, Asthme
  • Hearing loss, blind and learning problem

Trial locations and contacts

1 site in 1 country.

Thailand1 site
  • Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand

    Khon Kaen, Changwat Khon Kaen, 4002

Other trials in Thailand

About this study

Official title: Effect of Pre-operative Multimedia Physical Therapy Program in Open Heart Surgery: a Randomized Controlled Study

The goal of this clinical trial is to learn the effect of self prepare by multimedia program before going to heart surgery. The main questions it aim to answer is:

Is preparing for heart surgery on your own or with a physical therapist the same? Researchers were compare the effects of preoperative physical therapy between multimedia and traditional programs in patients undergoing open heart surgery.

Participants were received traditional therapy from a physical therapist or used a multimedia self-learning program.

Read the detailed description

This randomized controlled trial compared the effects of multimedia and traditional preoperative physical therapy programs in 70 patients undergoing elective open-heart surgery at Khon Kaen University, Thailand. Patients were divided equally into control and experimental groups. The control group received traditional therapy from a physical therapist, while the experimental group used a multimedia self-learning program. Both groups also received a leaflet with preoperative guidelines. After completing the programs, patients were assessed on chest expansion and surgery knowledge. Both groups showed significant improvement in upper and lower chest expansion after the programs. However, there were no significant differences between the groups in chest expansion or knowledge scores. The study concluded that a preoperative multimedia self-learning physical therapy program is as clinically effective as traditional therapy for patients preparing for open-heart surgery.

Being tested
Multimedia preoperative progarm, Traditional preoperative program

What participants receive

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

  • Multimedia preoperative progarmOther

    A two-dimensional (2D) animated video was developed to deliver educational content regarding open-heart surgery procedures (sternotomy and general anesthesia), the preoperative physical therapy program (diaphragmatic breathing, lower-lobe breathing, and chest expansion exercises), potential postoperative complications (e.g., pneumonia and atelectasis), therapeutic exercises (ankle pumping), and mobility training (bed mobility and transitioning from lying to a sitting position)

  • Traditional preoperative programOther

    traditional preoperative program from an experienced physical therapist

Study groups in NCT07814846
Study groupRoleWhat they receive
Control groupActive comparatorTraditional preoperative program from an experienced physical therapist
Receives: Other: Traditional preoperative program
Experimental groupExperimentalA two-dimensional (2D) animated video preoperative physical therapy program
Receives: Other: Multimedia preoperative progarm

What is being measured

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

  1. Chest expansion

    Chest expansion (both upper and lower) using a measuring tape

    Measured: Before and immediately after receiving the preoperative program

Secondary outcomes (1)
  1. Preoperative knowledge

    The secondary outcome was preoperative knowledge. Preoperative knowledge was assessed using a knowledge questionnaire, with scores ranging from 0 to 10. Higher scores indicated better knowledge.

    Measured: Immediately after receiving the preoperative program on the same day with chest expansion assessment.

Timeline

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

  1. First posted11 Sep 2026
  2. Study start17 Dec 2020
  3. Primary completion31 Dec 2023
  4. Study completion31 Dec 2023

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
The control groups received a traditional preoperative program from an experienced physical therapist and the experimental groups received a preoperative self-learning with multimedia program. All the patients in both groups also received the leaflet about preoperative program guidelines.
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07814846
Sponsor's protocol ID
CRprojectHE631569
Status last verified
Sep 2026
First submitted
22 Aug 2026
Last updated
11 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Multimedia preoperative progarm and Traditional preoperative program in people with Cardio Vascular Disease and Heart Surgery, run by Pajeemas Kittipanya-Ngam at 1 site in Thailand.

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 4 inclusion and 2 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 11 Sep 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 Thailand. 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?

Chest expansion (time frame: Before and immediately after receiving the preoperative program). 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 11 Sep 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in