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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03415230
Other study ID # AC-TMSQ-2018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date January 9, 2019

Study information

Verified date January 2019
Source Cyprus University of Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized control trial to test the effectiveness of therapeutic massage on the sleep quality and the stress levels in women that have completed their treatment for breast cancer.


Description:

The period following the completion of treatment for breast cancer (but also for any other type of cancer as well) is once that is accompanied by an increased uncertainty. This can often trigger increased anxiety levels and sleep disturbances. This trial tests the effectiveness of therapeutic massage as a non pharmaceutical intervention that can increase the management of stress and sleep disturbances during this period of time.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 9, 2019
Est. primary completion date December 20, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Women that completed their treatment

- women experiencing insomnia

- women experiencing anxiety

- women that speak and understand Greek

Exclusion Criteria:

- allergy to essential oils

- use of anticoagulants

- presence of edema

- presence of Varicose veins

Study Design


Intervention

Other:
Therapeutic massage
Massage therapy involves the administration of combinations of specific physical manipulations applied in a systematic way, with varying intensity, direction, rate, and rhythm, to the soft tissues of the body.
Sham massage
Sham massage involves only light touch massage in a non systematic way

Locations

Country Name City State
Cyprus Oncology Centre Nicosia

Sponsors (2)

Lead Sponsor Collaborator
Cyprus University of Technology Cyprus Anticancer Society

Country where clinical trial is conducted

Cyprus, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sleep Disturbances (insomnia) Athens insomnia scale (The AIS is a self-assessment psychometric instrument designed for quantifying sleep difficulty based on the ICD-10 criteria. It consists of eight items: the first five pertain to sleep induction, awakenings during the night, final awakening, total sleep duration, and sleep quality; while the last three refer to well-being, functioning capacity, and sleepiness during the day). Each item of the AIS can be rated 0-3, (with 0 corresponding to no problem at all and 3 to very serious problem); thus, the total score ranges from 0 (absence of any sleep-related problem) to 24 (the most severe degree of insomnia). Change from baseline total score at 4 weeks
Secondary Anxiety Hamilton Anxiety Rating Scale (HAM-A). The scale consists of 14 items. Each item is scored on a scale of 0 (not present) to 4 (severe), with a total score range of 0-56, where <17 indicates mild severity, 18-24 mild to moderate severity and 25-30 moderate to severe. Change from baseline total score at 4 weeks
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