NCT06946888

Brief 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. 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. 2.Original method group: followed the original self-coping method. 2. After the intervention began, participants completed study questionnaires weekly for two months.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 20, 2024

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 21, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 27, 2025

Completed
5 months until next milestone

Results Posted

Study results publicly available

October 6, 2025

Completed
Last Updated

October 6, 2025

Status Verified

September 1, 2025

Enrollment Period

6 months

First QC Date

April 21, 2025

Results QC Date

May 25, 2025

Last Update Submit

September 11, 2025

Conditions

Keywords

NursesAcupressureOccupational stressBurnout, professionalResilience, psychologicalAnxietyDepressionPsychological distress

Outcome Measures

Primary Outcomes (2)

  • Depressive Symptoms

    Depressive symptoms were assessed using the Taiwanese Depression Scale, which has demonstrated strong psychometric properties in Taiwanese populations. The TDS consists of 18 items rated on a 4-point Likert scale: 0 = none or seldom (less than one day per week), 1 = sometimes (one to two days per week), 2 = often (three to four days per week), and 3 = almost always (five to seven days per week). Total scores range from 0 to 54, with higher scores indicating greater severity of depressive symptoms. The results from Lee et al. (2000) demonstrated that the TDS had excellent reliability and validity. The Cronbach's alpha coefficient was 0.90, and the area under the receiver operating characteristic (ROC) curve was 0.92. The TDS also showed good concurrent validity, with a sensitivity of 0.89 and specificity of 0.92 at a cutoff score of 19. In the present study, the TDS demonstrated excellent internal consistency, with a Cronbach's alpha of .94.

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

  • Psychological Distress

    Psychological distress was measured using the Brief Symptom Rating Scale-5 (BSRS-5), a validated screening tool for general psychological distress. The BSRS-5 assesses the subjective severity of the following symptoms: (1) anxiety, (2) depression, (3) hostility, (4) low self-esteem, and (5) insomnia. Each symptom was scored on a 5-point Likert scale, ranging from 0 ("not at all") to 4 ("extremely"), with a total score ranging from 0 to 20 points. Higher scores indicate more severe psychological distress. Studies have shown that a total score of 3-4 is the optimal threshold for identifying clinically relevant distress based on receiver operating characteristic (ROC) curve analysis. The BSRS-5 showed high accuracy (AUC = 0.92) and good sensitivity (0.83) and specificity (0.86). Therefore, this study used a BSRS-5 total score ≥4 as one of the inclusion criteria to ensure that participants with at least mild psychological distress were included in the study.

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

Secondary Outcomes (5)

  • Resilience

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

  • Anxiety

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

  • Job Stress

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

  • Occupational Burnout

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

  • Emotional Distress

    At baseline(weeks 0) and once weekly for 8 weeks(weeks 1-8)

Study Arms (2)

Control group

NO INTERVENTION

Care continued in the original manner without any intervention.

Intervention group (Acupressure)

EXPERIMENTAL

Participants perform self-acupressure on the Shenmen and Neiguan points twice daily for 2 weeks.

Behavioral: Acupressure

Interventions

AcupressureBEHAVIORAL

Participants in this group will receive instruction on how to perform self-acupressure targeting two specific acupoints on the hands: Shenmen and Neiguan. The acupressure protocol includes pressing each acupoint approximately 15 times (about 30 seconds), with a total of four acupoints per session (both hands), for approximately 2 minutes per session. Pressure should be applied until a sensation of soreness, numbness, fullness, or slight pain is felt (equivalent to about 3 kg of pressure). Participants are asked to perform self-acupressure twice daily (once in the afternoon and once before bedtime, adjustable based on personal schedule) for a total of 2 weeks. They will record their practice using a daily log and continue to complete psychological and emotional outcome questionnaires weekly over a 2-month follow-up period.

Intervention group (Acupressure)

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kaohsiung Veterans General Hospital

Kaohsiung City, Zuoying District, 813414, Taiwan

Location

Related Publications (19)

  • Zhou XQ, Han YF, Xu MX. Effects of different intervention methods on psychological anxiety, stress, and fatigue among healthcare workers during COVID-19 pandemic: a systematic review and meta-analysis. Eur Rev Med Pharmacol Sci. 2024 Feb;28(4):1614-1623. doi: 10.26355/eurrev_202402_35491.

    PMID: 38436194BACKGROUND
  • Yang X, Liu Q, Wu X. Meta-Analysis of the Clinical Efficacy of Auricular Acupressure on Patients with Depression. Alpha Psychiatry. 2025 Feb 28;26(1):38776. doi: 10.31083/AP38776. eCollection 2025 Feb.

    PMID: 40110387BACKGROUND
  • Wu X, Tu M, Yu Z, Cao Z, Qu S, Chen N, Jin J, Xiong S, Yang J, Pei S, Xu M, Wang J, Shi Y, Gao L, Xie J, Li X, Fang J, Shao X. The efficacy and cerebral mechanism of intradermal acupuncture for major depressive disorder: a multicenter randomized controlled trial. Neuropsychopharmacology. 2025 Jun;50(7):1075-1083. doi: 10.1038/s41386-024-02036-5. Epub 2024 Dec 8.

    PMID: 39648209BACKGROUND
  • Peng Z, Zheng Y, Yang Z, Zhang H, Li Z, Xu M, Cui S, Lin R. Acupressure: a possible therapeutic strategy for anxiety related to COVID-19: a meta-analysis of randomized controlled trials. Front Med (Lausanne). 2024 Mar 21;11:1341072. doi: 10.3389/fmed.2024.1341072. eCollection 2024.

    PMID: 38576710BACKGROUND
  • Pachi A, Sikaras C, Melas D, Alikanioti S, Soultanis N, Ivanidou M, Ilias I, Tselebis A. Stress, Anxiety and Depressive Symptoms, Burnout and Insomnia Among Greek Nurses One Year After the End of the Pandemic: A Moderated Chain Mediation Model. J Clin Med. 2025 Feb 10;14(4):1145. doi: 10.3390/jcm14041145.

    PMID: 40004676BACKGROUND
  • Li J, Zhang K, Zhao T, Huang W, Hou R, Wang S, Zhao M, Guo Y. Acupressure for depression: A systematic review and meta-analysis. Asian J Psychiatr. 2024 Feb;92:103884. doi: 10.1016/j.ajp.2023.103884. Epub 2023 Dec 23.

    PMID: 38171225BACKGROUND
  • Hong WK, Kim YJ, Lee YR, Jeong HI, Kim KH, Ko SG. Effectiveness of electroacupuncture on anxiety: a systematic review and meta-analysis of randomized controlled trials. Front Psychol. 2023 Dec 19;14:1196177. doi: 10.3389/fpsyg.2023.1196177. eCollection 2023.

    PMID: 38173848BACKGROUND
  • Elliott D. Comparison of three instruments for measuring patient anxiety in a coronary care unit. Intensive Crit Care Nurs. 1993 Sep;9(3):195-200. doi: 10.1016/0964-3397(93)90027-u.

    PMID: 8400749BACKGROUND
  • Donovan KA, Grassi L, McGinty HL, Jacobsen PB. Validation of the distress thermometer worldwide: state of the science. Psychooncology. 2014 Mar;23(3):241-50. doi: 10.1002/pon.3430. Epub 2013 Nov 11.

    PMID: 25160838BACKGROUND
  • Dincer B, Inangil D. The effect of Emotional Freedom Techniques on nurses' stress, anxiety, and burnout levels during the COVID-19 pandemic: A randomized controlled trial. Explore (NY). 2021 Mar-Apr;17(2):109-114. doi: 10.1016/j.explore.2020.11.012. Epub 2020 Dec 3.

    PMID: 33293201BACKGROUND
  • Bal SK, Gun M. The effects of acupressure on pain, anxiety and vital signs in patients undergoing coronary angiography: A randomized and sham-controlled trial. Explore (NY). 2024 Jan-Feb;20(1):101-109. doi: 10.1016/j.explore.2023.07.001. Epub 2023 Jul 4.

    PMID: 37429762BACKGROUND
  • Amiri S, Mahmood N, Javaid SF, Khan MA. The Effect of Lifestyle Interventions on Anxiety, Depression and Stress: A Systematic Review and Meta-Analysis of Randomized Clinical Trials. Healthcare (Basel). 2024 Nov 13;12(22):2263. doi: 10.3390/healthcare12222263.

    PMID: 39595461BACKGROUND
  • Alghamdi R, Bahari G. Shift Work, Psychological Health Disorders, and Job Security Among Nurses: A Cross-Sectional Study. Healthcare (Basel). 2025 Jan 22;13(3):221. doi: 10.3390/healthcare13030221.

    PMID: 39942410BACKGROUND
  • Turkili S, Karaman A, Cam Yanik T, Altun Ugras G, Yuksel S, Turkili S, Tasdelen B. The Effects of Acupressure on Preoperative Anxiety, Postoperative Pain, and Nausea and Vomiting in Otolaryngology Patients. J Perianesth Nurs. 2025 Apr;40(2):385-392. doi: 10.1016/j.jopan.2024.05.027. Epub 2024 Sep 19.

    PMID: 39297814BACKGROUND
  • Zeiher W, Sego E, Trimmer D, Bowers C. Posttraumatic Stress Disorder in Nurses During a Pandemic: Implications for Nurse Leaders. J Nurs Adm. 2022 Feb 1;52(2):E3-E8. doi: 10.1097/NNA.0000000000001112.

  • Lin J, Chen T, He J, Chung RC, Ma H, Tsang H. Impacts of acupressure treatment on depression: A systematic review and meta-analysis. World J Psychiatry. 2022 Jan 19;12(1):169-186. doi: 10.5498/wjp.v12.i1.169. eCollection 2022 Jan 19.

  • Liang R, Tang L, Li L, Zhao N, Yu X, Li J, Wang Q, Cun H, Gao X, Yang W. The effect of pressing needle therapy on depression, anxiety, and sleep for patients in convalescence from COVID-19. Front Neurol. 2024 Dec 18;15:1481557. doi: 10.3389/fneur.2024.1481557. eCollection 2024.

  • Lee JI, Lee MB, Liao SC, Chang CM, Sung SC, Chiang HC, Tai CW. Prevalence of suicidal ideation and associated risk factors in the general population. J Formos Med Assoc. 2010 Feb;109(2):138-47. doi: 10.1016/S0929-6646(10)60034-4.

  • Katsiroumpa A, Moisoglou I, Papathanasiou IV, Malliarou M, Sarafis P, Gallos P, Konstantakopoulou O, Rizos F, Galanis P. Resilience and Social Support Protect Nurses from Anxiety and Depressive Symptoms: Evidence from a Cross-Sectional Study in the Post-COVID-19 Era. Healthcare (Basel). 2025 Mar 7;13(6):582. doi: 10.3390/healthcare13060582.

Related Links

MeSH Terms

Conditions

Anxiety DisordersDepressionOccupational StressBurnout, Professional

Interventions

Acupressure

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehaviorOccupational DiseasesStress, PsychologicalBurnout, Psychological

Intervention Hierarchy (Ancestors)

Therapy, Soft TissueMusculoskeletal ManipulationsComplementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Limitations and Caveats

1. The data are all self-administered questionnaires, which are affected by recall bias and social expectations. 2. The intervention period is only two weeks, and the intervention period or stimulation frequency can be extended. 3. Other acupoints related to emotional stability are not included, nor are they combined with common auxiliary methods. 4. Multiple workplace factors can be incorporated into the analysis to enhance external validity and reference for practical application.

Results Point of Contact

Title
Li-Ying Lin
Organization
Kaohsiung Veterans General Hospital

Study Officials

  • Li-Ying Lin, PhD

    supervise

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This is a single-center, randomized, single-blind, parallel-controlled trial. Eligible clinical nurses will be randomly assigned (1:1) to an intervention group or a control group. The intervention group will receive self-acupressure instructions on Shenmen and Neiguan points twice a day for two weeks, and record each treatment process. The control group will continue to use their usual stress and emotional distress coping strategies without any intervention. Both groups will be required to complete a validated questionnaire covering emotional distress, mood, anxiety, depression, stress, fatigue and resilience. Assessments will be conducted weekly for two months (including pre-test (baseline week 0) and follow-up for two months (weeks 1-8), a total of 9 times) to evaluate the effectiveness of self-acupressure compared with usual care.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Nursing Supervisor

Study Record Dates

First Submitted

April 21, 2025

First Posted

April 27, 2025

Study Start

June 20, 2024

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

October 6, 2025

Results First Posted

October 6, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations