Mode
Text Size
Log in / Sign up
N/A N=160 Randomized Single-blind Treatment

Effects of Acupressure on Nurses' Psychological Distress, Depression, Job Stress, Occupational Burnout, and Resilience

Psychological Distress · Anxiety · Depression · Nurses · Acupressure

Enrolled (actual)
160
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcome: Primary: Depressive Symptoms — 11.76; 11.55; 11.70; 10.84 score on a scale — p=0.837

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Acupressure (Behavioral)
Age
Adult, Older Adult · 20+ yrs
Sex
All
Sponsor
Kaohsiung Veterans General Hospital.
Primary completion
Dec 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Depressive Symptoms
11.76; 11.55; 11.70; 10.84; 12.05; 10.86 0.837
PRIMARY
Psychological Distress
5.65; 5.54; 5.54; 5.31; 5.05; 4.6 0.63
SECONDARY
Resilience
38.64; 39.18; 38.83; 39.62; 38.86; 39.63 0.333
SECONDARY
Anxiety
45.18; 44.19; 44.64; 43.36; 43.93; 41.78 0.857
SECONDARY
Job Stress
45.80; 45.10; 45.98; 45.63; 45.64; 44.90 0.636
SECONDARY
Occupational Burnout
48.20; 49.05; 48.60; 48.44; 46.53; 46.46 0.593
SECONDARY
Emotional Distress
3.95; 3.84; 3.59; 3.43; 3.41; 3.18 0.913

Summary

This measurement aims to understand the effect of self-acupressure on the Shenmen Point (神門) and (內關) points on the hand on emotional distress, anxiety, depression, stress, work fatigue and adaptability of clinical nurses. The main questions it aims to answer are: Whether acupressure can reduce emotional distress, anxiety, depression, stress and work fatigue in nursing staff. Participants will: 1. Enforcement measures: 1. Acupressure group: Perform self-acupressure twice a day, each time for about 2 minutes, and record the acupressure records every day for 2 consecutive weeks. 2. Original method group: followed the original self-coping method. 2. After the intervention began, participants completed study questionnaires weekly for two months.

Eligibility Criteria

Inclusion Criteria

  • Clinical nurses aged 20 years or older from a designated medical center.
  • Nurses who score ≥3 on the emotional distress thermometer or ≥4 on the Brief Symptom Rating Scale (BSRS-5) based on self-reported questionnaires.
  • Able and willing to complete the required study questionnaires during the 2-month study period.

Exclusion Criteria

  • Nurses who refuse to participate after being informed about the study or are unable to comply with the study protocol.
  • Nurses working in non-patient-care units (e.g., administrative departments or supply centers).
  • Pregnant nurses.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06946888). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search