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AA on Drug Abusers by Nursing Students

Around the Turn: A Feasibility Cluster Randomized Controlled Trial of Using Auricular Acupressure to Abstain From Drug Abuse Through Training Nursing Students

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05877742
Enrollment
80
Registered
2023-05-26
Start date
2023-03-20
Completion date
2025-06-20
Last updated
2025-04-20

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

Conditions

Drug Abuse

Keywords

Auricular Acupressure, Nursing Students

Brief summary

Drug abuse is a serious public health issue. Despite the serious consequences of drug abuse, there are around 2000 new cases reported by drug abusers each year. There is growing evidence of the use of auricular acupressure (AA), a traditional Chinese medicine (TCM) treatment modality, in reducing withdrawal symptoms among drug abusers. This study aims to investigate the feasibility and effectiveness of training nursing students to deliver brief education on AA on drug abusers.

Detailed description

A 2-arm feasibility cluster RCT will be conducted in the 80 drug abusers from 7 substance abuse clinics in Hong Kong Hospital Authority following the CONSORT statement. The intervention group will receive AA intervention individually from trained nursing students. The control group will individually receive a 5-minute seminar delivered by a research assistant.

Interventions

OTHERAA group

Participants will individually receive a 5-minute AA education delivered verbally at his/her respective clinic by a trained nursing student interventionist in addition to the usual scheduled follow-ups and activities at clinics.

OTHERControl group

To mimic the time and attention spent, the control group will individually receive a 5-minute seminar delivered by an RA.

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 or above * Have reported to abuse drugs within the past 30 days * Can communicate in Cantonese and read Chinese

Exclusion criteria

* Unstable mental conditions that are not suitable for the intervention * Receiving acupuncture or acupressure treatment currently or in the previous 30 days

Design outcomes

Primary

MeasureTime frameDescription
Adverse eventsat the 6-month follow-updefined as unfavorable and unintended events that are not present at baseline, or appear to have worsened during the study.
Attendance rateat the 6-month follow-upcalculated by dividing the number of abusers who complete the intervention by those who are randomized.
Retention rateat the 6-month follow-up: calculated by dividing the number of abusers who remain in the study by those who are randomized. Retention rates for the intervention and control groups will be calculated at each follow-up.
Adherence to intervention protocolat the 6-month follow-upcalculated by dividing the number of abusers who follow the intervention protocol by those who are randomized.
Complete rateat the 6-month follow-upcalculated by dividing the number of abusers who returned questionnaires by the number of questionnaires distributed. This will be calculated by groups at baseline and each follow-up.
Missing dataat the 6-month follow-upcalculated as the percentage of missing values in the dataset. Unknown or blank values will be considered missing values.
Screening rateat the 6-month follow-upcalculated as the number of abusers screened at participated clinics divided by number of abusers at participated clinics during the recruitment period.
Eligibility rateat the 6-month follow-upcalculated by dividing the number of abusers who are eligible by the number who are screened.
Consent rateat the 6-month follow-upcalculated by dividing the number of abusers who consent to join the study by the number who are eligible.
Randomization rateat the 6-month follow-upcalculated by dividing the number of abusers who are randomized into intervention and control groups by those who provide consent.

Secondary

MeasureTime frameDescription
Abstinence with urine testingat the 6-month follow-up. Those who report no drug abuse within the past 30 days at the 6-month follow-up will be further invited for urine testing.
Self-reported levels of cravingat the 6-month follow-upThe Chinese version of the 3-item craving scale will be used to measure abusers' self-reported levels of craving.
Anxietyat the 6-month follow-upGeneralized anxiety disorder-7 will be used to measure the severity of self-reported anxiety.
Quality of life measures by short-Form Six-Dimensionat the 6-month follow-upShort-Form Six-Dimension will be used to assess abusers' quality of life.It contains six dimensions of health. The Chinese version is well validated in Hong Kong.
Self-reported abstinenceat the 6-month follow-upSelf-reported drug abstinence at last 30 days.

Countries

Hong Kong

Contacts

Primary ContactKa Wai Katherine Lam
kw-katherine.lam@polyu.edu.hk27666420
Backup ContactKa Yan Ho
kyeva.ho@polyu.edu.hk2766417

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026