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Virtual Reality Therapy and Non-Sleep Deep Rest Relaxation After Joint Arthroplasty

W

Wroclaw University of Health and Sport Sciences

Status

Active, not recruiting

Conditions

Osteoarthritis, Hip
Osteoarthritis, Knee
Arthropathy

Treatments

Behavioral: Conventional rehabilitation
Behavioral: Non-Sleep Deep Rest Relaxation
Device: Immersive Virtual Reality Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT07386561
KE-U/108/2025

Details and patient eligibility

About

The aim of this study is to compare the effectiveness of Virtual Reality therapy (VR therapy), Non-Sleep Deep Rest relaxation (NSDR relaxation) each delivered as an adjunct to standard postoperative rehabilitation, in older adults following hip or knee arthroplasty, focusing on reducing psychological stress and improving functional recovery.

Full description

Older adults undergoing hip or knee arthroplasty frequently experience psychological distress, including elevated stress and anxiety, which may reduce engagement in rehabilitation and limit functional recovery. This randomized clinical trial will compare the effectiveness of Virtual Reality therapy (VR therapy) and Non-Sleep Deep Rest relaxation (NSDR relaxation) each delivered as an adjunct to standard postoperative rehabilitation, in this population. Ninety participants aged 60-85 years, within three months post-arthroplasty, will be recruited from an inpatient rehabilitation unit and randomized to receive standard rehabilitation alone, standard rehabilitation plus VR therapy or standard rehabilitation plus NSDR relaxation over a four-week period. The VR therapy will consist of eight 20-minute session using VRTierOne medical device. NSDR relaxation will be delivered as eight 20-minute, audio-guided relaxation sessions (body scan and breathing exercises) via noise-cancelling headphones in a quiet environment. Primary outcomes will include changes in psychological distress (stress, anxiety, depressive symptoms; assessed with validated questionnaires) and functional recovery (functional performance and mobility indices), measured at baseline and post-intervention. Both adjuncts are designed to be safe, well-tolerated, and feasible for clinical implementation. The findings are expected to clarify the comparative role of VR therapy and NSDR relaxation as low-risk adjunctive strategies to support psychological well-being and functional outcomes during post-arthroplasty rehabilitation.

Enrollment

90 estimated patients

Sex

All

Ages

60 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Individuals aged 60 years and above who have recently (within the past 3 months) undergone knee or hip joint arthroplasty surgery.

Exclusion criteria

  • Hearing impairment preventing the use of audio recordings;
  • Cognitive impairment precluding independent completion of study questionnaires;
  • History of disorders of consciousness, psychotic symptoms, bipolar disorder, or other severe psychiatric disorders;
  • Current use of psychoactive medications;
  • Ongoing psychiatric treatment or participation in individual psychological therapy;
  • Functional status precluding independent ambulation (e.g., wheelchair-bound or bedridden; use of orthopedic aids such as crutches or a walker is permitted);
  • Withdrawal of consent or refusal to participate at any stage of the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

90 participants in 3 patient groups

Immersive Virtual Reality Therapy Group
Experimental group
Description:
Conventional orthopedic rehabilitation supplemented by VR therapy
Treatment:
Device: Immersive Virtual Reality Therapy
Behavioral: Conventional rehabilitation
NSDR Group
Experimental group
Description:
Conventional orthopedic rehabilitation supplemented by non-sleep deep rest relaxation
Treatment:
Behavioral: Non-Sleep Deep Rest Relaxation
Behavioral: Conventional rehabilitation
Conventional Rehabilitation Group
Active Comparator group
Description:
Conventional orthopedic rehabilitation
Treatment:
Behavioral: Conventional rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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