NCT01178775

Brief Summary

The aims of this three-year study are to:

  1. 1.develop and validate a perceived meaning of fatigue scale
  2. 2.examine the effect of individualized patient education and walking programs on alleviating fatigue in patients with gastric or colorectal cancer,and further explore the relationship between the perceived meaning of fatigue and intervention outcome.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
105

participants targeted

Target at P25-P50 for not_applicable gastric-cancer

Timeline
Completed

Started Sep 2008

Typical duration for not_applicable gastric-cancer

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2008

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2010

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

April 11, 2010

Completed
4 months until next milestone

First Posted

Study publicly available on registry

August 10, 2010

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

August 10, 2010

Status Verified

August 1, 2010

Enrollment Period

1.5 years

First QC Date

April 11, 2010

Last Update Submit

August 9, 2010

Conditions

Gastric Cancer

Keywords

fatiguemeaningeducationwalking program

Outcome Measures

Primary Outcomes (1)

  • Fatigue Symptom Inventory

    the level of fatigue in three groups will be measured at the end of intervention

    Time point(s) at which outcome measure is assessed at 16 Weeks after recruting in this study .

Study Arms (3)

1

NO INTERVENTION

control design

2

NO INTERVENTION

education only group

3

EXPERIMENTAL

education and education and walking program design

Behavioral: walking

Interventions

walkingBEHAVIORAL

use a pedometer for records steps.

3

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • The patients with gastric cancer during receiving chemotherapy
  • Those who are willing to participate in the research
  • Aged above 18

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan

RECRUITING

MeSH Terms

Conditions

Stomach NeoplasmsFatigue

Interventions

Walking

Condition Hierarchy (Ancestors)

Gastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesStomach DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

LocomotionMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological PhenomenaExerciseMotor Activity

Study Officials

  • Shiow-Ching Shun, Ph.D

    National Taiwan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Shiow-Ching Shun, Ph.D

CONTACT

886-2-2312-3456scshun@ntu.edu.tw

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

April 11, 2010

First Posted

August 10, 2010

Study Start

September 1, 2008

Primary Completion

March 1, 2010

Study Completion

December 1, 2011

Last Updated

August 10, 2010

Record last verified: 2010-08

Locations

TW(1)