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A Study of Dose-response Relationship and the Evidence Based Multisensory Stimulation Intervention

NCT05012709 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 95

Last updated 2021-08-19

No results posted yet for this study

Summary

Design: This parallel randomized controlled trial (RCT) was conducted according to the Consolidated Standards of Reporting Trials (CONSORT).

Methods: In total, 90 patients were randomly assigned to either the intervention or the control group. After a 2-week washout period, the intervention group was reassigned to the control and vice versa. The CONSORT checklist for RCT was reported. Psychotic symptoms, emotional reactions, behavioral relaxation responses and heart rates were assessed at 6 time points.

Conditions

  • Psychotic Disorders
  • Anxiety
  • Complementary Therapies
  • Clinical Trial

Interventions

BEHAVIORAL

multisensory stimulation therapy

The intervention group received six 30-minute MST sessions. During MST session, participants can choose their preferred sensory stimuli such as essential oil diffuses, music and so on.

Sponsors & Collaborators

  • Taiwan Nurses Association

    collaborator OTHER

  • National Cheng Kung University

    collaborator OTHER

  • Jianan Psychiatric Center, Ministry of Health and Welfare

    lead OTHER

Principal Investigators

  • Mei-Feng Lin, PhD · National Cheng Kung University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-15
Primary Completion
2013-01-10
Completion
2013-03-10

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05012709 on ClinicalTrials.gov