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Self-acupuncture for Migraines Feasibility Study (SAM)

U

University of West London

Status and phase

Invitation-only
Phase 2
Phase 1

Conditions

Migraine

Treatments

Device: Acupuncture

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Patients who have had a course of acupuncture at the Royal London Hospital for Integrated Medicine to manage their migraines, and found it effective, will be taught to do self-acupuncture. This is a feasibility study so the main aim is to test the trial design but the researchers will also explore self-acupuncture's effectiveness, acceptability and safety.

Full description

Aim: The proposed study will evaluate the feasibility of teaching SA to patients with migraines in the United Kingdom National Health Service setting.

Methodology: The study will employ a pragmatic, mixed-methods, randomised, parallel-group, exploratory design. The study will compare SA plus standard care versus standard care alone. Participants will complete outcome measures at various time points and be invited to take part in a qualitative telephone interview to explore their views on the design of the study and acceptability of the intervention. The researcher will take field notes of the observation of the SA teaching session to explore the acceptability of the SA teaching method. Data will be analysed to test the hypothesis.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients aged 18 years old and over.
  • Patients with migraines (when topiramate and propranolol are unsuitable).
  • Patients who have been referred to the Royal London Hospital for Integrated Medicine (RLHIM) for a course of at least 6 acupuncture sessions to manage their migraines.
  • Patients who have completed a course of acupuncture for the management of their migraines at RLHIM and self-declare that they benefitted from it.
  • Patients must have completed the course of acupuncture within the last 3 to 24 months.

Exclusion criteria

  • Patients unwilling to participate (for instance due to needle phobia).
  • Patients currently receiving acupuncture.
  • Patients with severe clotting dysfunction or who bruise spontaneously.
  • Patients unable to complete the questionnaires as judged by the researchers.
  • Patients who have previously been taught or have practiced SA.
  • Patients who are assessed as being unable to do SA (such as if they have poor hand function).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

self-acupuncture plus usual care
Active Comparator group
Description:
Participants will be taught to do self-acupuncture to manage their migraines. They can also do all the other things they normally do to manage their migraines apart from having acupuncture elsewhere.
Treatment:
Device: Acupuncture
usual care
No Intervention group
Description:
Participants can do all the other things they normally do to manage their migraines apart from having acupuncture elsewhere.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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