ClinicalTrials.Veeva

Menu

Exercises Using Virtual Reality on Cancer Patients

U

University of Hail

Status

Completed

Conditions

Breast Cancer Female

Treatments

Other: exercises using virtual reality technology

Study type

Interventional

Funder types

Other

Identifiers

NCT06058936
H-2023-366

Details and patient eligibility

About

in this study, a randomized controlled trial will be conducted to evaluate the effect of adding exercises using virtual reality on achievements in patients having breast cancer and conducted surgical treatment

Full description

in this study, a randomized controlled trial will be conducted to evaluate the effect of adding exercises using virtual reality on achievements in patients having breast cancer and conducted surgical treatment.

A virtual reality (VR) environment is created by combining computer systems and sensor technology with the use of three-dimensional graphics and enabling users to experience a more real, immersive experience by utilizing their various senses (vision, hearing, touch, etc.) through the use of the computer and sensor technologies and it is characterized by immersion, imagination, and interaction 2 groups will be selected randomly to receive experimental and control intervention for 1 month and outcomes will be collected before and after treatment.

Enrollment

54 patients

Sex

Female

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Breast cancer female patients
  • Age ≥40 years
  • All patients with Eastern Cooperative Oncology Group performance status score ≤ 2
  • Having to undergo primary treatment with surgery, chemotherapy, and/or radiotherapy based on the patient's need

Exclusion criteria

  • Severe anemia (Hb ≤ 8 g/dL)
  • Uncontrolled hypertension, diabetes
  • severe infection, neurologic or muscular diseases prohibiting physical activity
  • severe heart disease or myocardial infarction during the last six months, and a severe chronic obstructive pulmonary disease
  • uncontrolled and/or extensive brain metastases, or bone metastases that were assessed to pose a risk of pathological fractures from exercising
  • Contraindications given by the physician

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

virtual reality
Experimental group
Description:
The patients in this group are under exercise training and pneumatic pressure followed by Pablo©Handle training for 45 minutes per week for 8 week -Pablo©Handle training One-dimensional therapy games using five games are available for Pablo©Handle which are (Recycle, Firefighters, Shooting Cans, Balloon, and Apple hunter) The session will be 3 min for each game about 15 min for each session 3 times per week for 8 week
Treatment:
Other: exercises using virtual reality technology
regular exercises
Active Comparator group
Description:
The patients in this group will receive exercise training and pneumatic pressure only for 30 min3 times per week for 8 week * Exercise training will be done by the following exercise for 15 min3 times per week for 8 week * Intermittent Compression Therapy Parameters: using the (Care Pump expert 8) * Pressure. 60 mmHg, Direction. Distal to proximal, Speed 4 to 5, for 15 min /3 times per week for 8 week
Treatment:
Other: exercises using virtual reality technology

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems