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Application of Real-time Facial Motion Tracking Feedback AR Adjuvant Therapy for Nasopharyngeal Carcinoma Patients Based on Health Belief Model

Application of Real-time Facial Motion Tracking Feedback AR Adjuvant Therapy for Nasopharyngeal Carcinoma Patients Based on Health Belief Model

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090305
Enrollment
Unknown
Registered
2024-09-27
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nasopharyngeal Carcinoma

Interventions

The Control Group:Participants in the control group, the routine care group, were told the benefits of regular mouth exercises and asked to maintain their old habits. The duration and intensity of the
The Intervention Group:The application intervention group used the health application intervention app we developed to intervene for 30 minutes each time. All subjects were asked not to seek any other

Sponsors

The Shanghai Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: The study population included patients with nasopharyngeal carcinoma recruited from the cancer hospital through posters and questionnaires. They had completed radiotherapy and chemotherapy and were ready to be discharged. The inclusion criteria are as follows : (1) Patients with nasopharyngeal carcinoma diagnosed by pathology or histology, and prescription of radiotherapy and chemotherapy ;(2) 35 = age = 55 years old ; (3) Patients understand their own condition ; ( 4 ) Patients provide informed consent and are willing to participate in this study ; (5) Patients can use smart phones and WeChat applications ; (6) Functional status score ( KPS ) 80-100 and Eastern Cooperative Oncology Group ( ECOG ) 0-5.

Exclusion criteria

Exclusion criteria: Exclusion criteria are as follows : (1) Severe cognitive impairment or mental disorders ; (2) Inability to exercise ( due to potential heart, nerve, muscle and / or joint diseases ) ; (3) History of radiotherapy and chemotherapy ; (4) Participated in relevant mouth exercise ( routine nursing, follow-up video, etc. ).

Design outcomes

Primary

MeasureTime frame
Maximum mouth opening data;Evaluation of mouth opening symmetry;Training frequency ( per week );HBMQ Questionnaire;

Secondary

MeasureTime frame
Borg Rating of Perceived Exertion Scale, BRPE;Health-related quality of life;System Usability ;

Countries

China

Contacts

Public ContactXiaoyan Meng

The Shanghai Cancer Center

mengxiaoyan1973@163.com+86 180 1731 7399

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 12, 2026