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Laser Auriculotherapy for management of neuropsychological symptoms in patients with gastrointestinal Cancer

Effect of Laser Auriculotherapy on the management of cluster of neuropsychological symptoms in patients with gastrointestinal Neoplasms: randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9pvbx34
Enrollment
Unknown
Registered
2024-11-12
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Gastrointestinal Neoplasms

Interventions

This is a two-arm, double-blind, randomized controlled clinical study carried out with patients diagnosed with gastrointestinal cancer undergoing chemotherapy treatment. 52 participants will be recrui
E02.594.540

Sponsors

Programa de Pós-Graduação em Enfermagem - Universidade Federal do Rio Grande do Norte
Lead Sponsor
Universidade Federal do Rio Grande do Norte
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients of both sexes and any gender; aged at least 18 years; with gastrointestinal cancer; who will begin treatment with chemotherapy

Exclusion criteria

Exclusion criteria: Patients who have a disorder that makes it impossible to understand and participate in the research; patients who already use the complementary therapy used in the study; patients who have an infectious process or lesion in the ear; refusal to receive laser ear treatment; patients with disease recurrence

Design outcomes

Primary

MeasureTime frame
Reduction in anxiety scores measured using the instrument: Beck Anxiety Inventory (BAI); reduction in scores related to fatigue measured by the Piper Fatigue Scale and reduction in scores related to sleep, using the Pittsburgh Sleep Quality Index.

Secondary

MeasureTime frame
Physiological parameters will be evaluated during laser auriculotherapy sessions: heart rate (HR), respiratory rate (RR) and Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP), temperature (T) and oxygen saturation (Sat02), before and after each intervention in all sessions.

Countries

Brazil

Contacts

Public ContactDaniele Vieira Dantas

Universidade Federal do Rio Grande do Norte

daniele00@hotmail.com+55-84-999367260

Outcome results

None listed

Source: REBEC (via WHO ICTRP)