Development of an Informed Consent Statement Which Communicates the Risk of Adverse Events Associated With Dry Needling (DNICNGT)

Youngstown State University

Status: Completed

Conditions: Dry Needling

Treatments: Other: Nominal Group Technique - 2 to 3 hour virtual meeting

Study type: Observational

Funder types: Other

Identifiers

NCT05560100

2022-173

Details and patient eligibility

About

As Dry Needling (DN) continues to see increased use in the clinic, there is a need to establish adverse events that could occur as a result of DN intervention. The adverse events are important to consider when an individual needs to make an informed decision regarding their care. It is important to consider how such information should be presented during the informed consent process to improve an individual's ability to make a sound decision regarding their own personal care.

Full description

Dry Needling (DN) has been defined by a Task Force organized by the Federation of State Boards of Physical Therapy (FSBPT) as "a skilled intervention performed by a physical therapist using filiform needles to penetrate the skin and/or underlying tissues to affect change in body structures and functions for the evaluation and management of neuromusculoskeletal conditions, pain, movement impairments, and disability". As DN interest continues to expand and studies continue to show the feasibility of applying DN to a wider range of pathological conditions, there is a need to understand the risks related to the use of DN. Understanding the risks associated with DN will allow for improvements in clinical decision making regarding it's application in the clinic.

Enhancing patient choice is a central theme of medical ethics and law. Informed consent (IC) is the legal process used to promote patient autonomy while concepts of shared decision making (SDM) is a widely promoted ethical approach. IC is a means of respecting the autonomous preferences of persons seeking health care or participation in research. Empowerment of the patient is important in healthcare and can lead to improvements in overall quality of patient care and outcomes.

To date, there has been little research conducted that explored the topic of how risks should be presented during the IC process. The purpose of this study will be to utilize expert consensus to establish a risk statement for adverse events associated with DN that an be used during IC.

Enrollment: 5 patients

Sex: All

Ages: 18 to 100 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Participants must be 18 years old or above and be able to read/write in English Participants must provide informed consent Participants must meet the criteria of one of the previously defined cohort groups used in the study

Dry Needling Experts

(1) Must have >= 5 years of clinical practice performing dry needling and at least ONE of the following secondary criteria:

1. Certification in Dry Needling
2. Completion of a manual therapy fellowship that included dry needling training
3. >= 1 total scholarly product (poster presentation, author of a peer-reviewed publication) involving the use of dry needling

Legal Expert

An individual who is an attorney and who has had training in health law as evidenced by at least ONE of the following criteria:

1. Training in health law as evidenced by ONE of the following:

   1. Concentration/Certification in Health Law
   2. L.L.M in health or medical law
   3. SJD in health law

2. Experience in litigating medical malpractice cases involving failure to obtain informed consent

3. Published scholarship on informed consent in an academic journal (>= 1) Policy Expert

An individual who has a degree in bioethics with at least ONE of the following criteria:

1. >= 5 years of experience in obtaining informed consent or an advanced graduate degree in bioethics
2. Has served on ethics related committee in a healthcare institution or healthcare society/professional association
3. Is or has been a member of a state licensing board

Patient Must have participated in >= 1 session of dry needling treatment and not be a healthcare provider

Exclusion criteria

Participants who did not provide informed consent Participants who did not meet the inclusion criteria of one of the four cohort groups defined in the study.

Trial design

5 participants in 4 patient groups

Patients

Description:

Must have participated in \>= 1 session of dry needling treatment and not be a healthcare provider.

Treatment:

Other: Nominal Group Technique - 2 to 3 hour virtual meeting

Dry Needling Experts

Description:

(1) Must have \>= 5 years of clinical practice performing dry needling and at least ONE of the following secondary criteria: 1. Certification in Dry Needling 2. Completion of a manual therapy fellowship that included dry needling training 3. \>= 1 total scholarly product (poster presentation, author of a peer-reviewed publication) involving the use of dry needling

Treatment:

Other: Nominal Group Technique - 2 to 3 hour virtual meeting

Policy Experts

Description:

An individual who has a degree in bioethics with at least ONE of the following criteria: 1. \>= 5 years of experience in obtaining informed consent or an advanced graduate degree in bioethics 2. Has served on ethics related committee in a healthcare institution or healthcare society/professional association 3. Is or has been a member of a state licensing board

Treatment:

Other: Nominal Group Technique - 2 to 3 hour virtual meeting

Legal Experts

Description:

An individual who is an attorney and who has had training in health law as evidenced by at least ONE of the following criteria: 1. Evidence of training based on ONE of the follow: 1. Concentration/Certification in Health Law 2. L.L.M in health or medical law 3. SJD in health law 2. Experience in litigating medical malpractice cases involving failure to obtain informed consent 3. Published scholarship on informed consent in an academic journal (\>= 1)

Treatment:

Other: Nominal Group Technique - 2 to 3 hour virtual meeting