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An intervention study to the physical activity program for improving the sleep quality of cancer Survivor's

An intervention study to the physical activity program for improving the sleep quality of cancer Survivor's - An intervention study for improving the sleep quality of cancer Survivor's

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025805
Enrollment
50
Registered
2017-02-10
Start date
2017-02-10
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cancer

Interventions

Implementation Activity Program

Sponsors

Fukuoka University Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patient of hematopoietic neoplasms and gastrointestinal cancer 2)Patient have received the chemotherapy and the supportive treatment. (those who have carried out the symptom control by medication of a hypertension, a DM, etc. are involves to a subject). 3) Patient has poor sleep quality of PSQI-J scores greater than 6 4) Patient who can communicate others and consciousness 5) Performance Status 0-2 6) 20 -65 years old 7) Patient who can detach and attach a actigraph and an accelerometer by myself

Exclusion criteria

Exclusion criteria: 1) Patient by whom a psychological burden is judged to be a gain by attend of a survey 2)Patient of a cutaneous sensitization 3)Patient by whom an everyday physical activity is restricted (arrhythmia, ischemic heart disease, and heart failure are exist patients etc) 4)Patient has bone metastasis and motor disturbance 5)Patient who not desirable by researcher's judged

Design outcomes

Primary

MeasureTime frame
the subjective sleep by PSQI-J the objective sleep by Acitygraph First: before intervention Second: 2 week after intervention Third: 4 week after intervention Fourth: 8 week after intervention

Secondary

MeasureTime frame
the amount of body activities the fatigue by CFS HRQOL by sf-36 a subjective symptom a hematometry datum

Countries

Japan

Contacts

Public ContactAyako Ura

Fukuoka University Faculty of Medicine, School of Nursing

ayako@adm.fukuoka-u.ac.jp092-801-1011

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026