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Study of Inspiratory Muscle Training for Patients Undergoing Esophageal Surgery

Mayo Clinic logo

Mayo Clinic

Status

Withdrawn

Conditions

Neoplasms, Esophageal
Esophagus Cancer
Cancer of the Esophagus
Esophageal Cancer
Cancer of Esophagus
Esophagus Neoplasm

Treatments

Other: Questionnaires
Behavioral: Inspiratory Muscle Training-Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT02843750
15-009190

Details and patient eligibility

About

To obtain definitive evidence for the effectiveness of a short preoperative inspiratory muscle training (IMT) protocol on the morbidity and recovery from an esophageal surgical resection.

Sex

All

Ages

40 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients diagnosed with esophageal cancer and scheduled for esophageal resection at the Mayo Clinic Rochester with gastric conduit reconstruction -Cognitively capable to understand and perform a preoperative program
  • Able to follow the intervention program for at least 2 weeks before surgery (surgery is usually scheduled 4 to 12 weeks after radiation)
  • Willing to sign the informed consent form

Exclusion criteria

  • Unable to communicate in the English language
  • Participating in a conflicting trial concerning esophageal resection

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Inspiratory Muscle Training-Rehabilitation
Experimental group
Description:
Patients will start the IMT-R, following their consent and within 2 weeks of their scheduled surgery: 10 sessions lasting about 90 minutes. Participants who completed their initial IMT greater than 2 weeks prior to surgery will have an additional visit prior to surgery. Participants will receive a Participant Manual demonstrating and explaining the rehabilitation process. Participants will also receive a log for recording their efforts and notes. A DVD of the rehabilitation is available to the participant. Participants will complete questionnaires at baseline and 3 months.
Treatment:
Other: Questionnaires
Behavioral: Inspiratory Muscle Training-Rehabilitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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