The Effects of Intra Operative Hand Reflexology for Patients Receiving Out Patient Vein Surgery

The Whiteley Clinic

Status: Completed

Conditions: Anxiety; Pain

Treatments: Behavioral: Hand Reflexology

Study type: Interventional

Funder types: Other

Identifiers

NCT01663025

WC1HM

Details and patient eligibility

About

This randomised controlled trial aims to compare the effectiveness of hand reflexology received during office based vein surgery, under local anaesthetic on patient's reports of pain and anxiety, compared to usual standard care.

Full description

The negative effects of anxiety and pain on surgical recovery are well documented. It is also accepted that distraction can be effective in pain reduction. This randomised controlled trial will explore the effect of intra operative hand reflexology on pain perception and anxiety during office-based surgery under local anaesthetic. Participants will be randomly allocated to either the experimental condition, in which they will receive a hand reflexology during treatment, or control condition in which they will receive usual standard care. Immediate and longer term outcomes will be explored.

Eight weeks after surgery, participants will return to the clinic for a follow up appointment. While they are in the waiting area they will be asked to complete a short questionnaire to assess time taken to return to pre surgical levels of functioning, pain experienced in the first four weeks after surgery, severity of venous symptoms and satisfaction with treatment.

Enrollment: 100 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• To be aged between 18 and 80
• To be able to give informed consent
• To be receiving, endovenous laser ablation or phlebectomies for the treatment of varicose veins
• To have a good understanding of written and spoken English.
• To arrive at the clinic with sufficient time before their procedure to give consent and complete the questionnaire (>20 mins)

Exclusion criteria

-To be aged under 18 or over 80

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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100 participants in 2 patient groups

Hand Reflexology

Experimental group

Description:

Participants in this condition will receive hand reflexology, performed by a trained reflexologist during their treatment. This will be in addition to usual standard care therefore the surgeon will speak to the participant occasionally to ensure they are comfortable.

Treatment:

Behavioral: Hand Reflexology

Control

No Intervention group

Description:

Participants in condition will form the control group for the study. They will receive usual standard care during treatment which will involve the surgeon speaking to them occasionally to ensure that they are comfortable.