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The Recovery of Reaching Movement in Breast Cancer Survivors: Two Different Rehabilitative Protocols in Comparison

CompletedNot applicableNCT04166279
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This study emphasizes the importance of rehabilitation in breast cancer survivors after mastectomy, even during the course of radiotherapy and chemotherapy, both for good efficacy in reducing pain and for functional recovery of the upper limb. Authors designed a randomized-controlled trial to compare two different rehabilitation protocols: the single rehabilitative treatment (ST) and the group treatment (GT). The study is the first attempt to measure the reaching movement after BC surgery with an optoelectronic evaluation system previously standardized in the neurological field during rehabilitation treatment.

Study details

Official title
The Recovery of Reaching Movement in Breast Cancer Survivors: Two Different Rehabilitative Protocols in Comparison
Conditions
Interventions
  • Other: Single rehabilitative treatment
  • Other: Group rehabilitative treatment
Sponsor
University of Roma La Sapienza
Start date
2018-01-08
Primary completion
2019-04-15
Sex
Female
Age range
from 18 Years to 60 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Italy
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * total mastectomy carried out 12 months prior to recruitment for rehabilitation with breast prostheses or tissue expanders performed * age from 18 to 60 years * body mass index (BMI) \< 30 * no cognitive dysfunctions ( Mini Mental State Examination MMSE \> 24) Exclusion Criteria: * presence of lymphangitis or mastitis * presence of metastasis * surgical complications * neurological deficits * shoulder joint problems before surgery * severe-moderate lymphedema and web axillary syndrome * visual problem not corrected by lenses

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04166279