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Implementation and Evaluation of an Activity Program to Improve Quality of Life Outcomes in Women Diagnosed With Cancer

Implementation and Evaluation of an Activity Based Program to Improve Quality of Life Outcomes in Women Diagnosed With Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02802787
Enrollment
92
Registered
2016-06-16
Start date
2016-06-30
Completion date
2019-08-31
Last updated
2020-04-15

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

Conditions

Cancer

Keywords

Quality of life, Occupation, Pain, Fatigue

Brief summary

Implementation and Evaluation of an Activity Based Program to Improve Quality of Life, Pain and Fatigue Outcomes in Women Diagnosed With Cancer. Demonstrate improved life satisfaction, decreased pain and decreased fatigue (with evidenced gathered at three consecutive periods Quality of Life, Pain and Fatigue surveys).

Detailed description

This research study will focus on developing and implementing two one-week activity camps in the summer of 2016 for women diagnosed with cancer. One camp will be held in West Philadelphia and another in Camden, New Jersey, both of which have been identified as underserved areas for health access. The focus of this programming is to allow women to engage in activities they may not be engaged in since the diagnosis of cancer and to provide them with opportunities to socially interact and communicate with individuals who may have encountered the same difficulties as them. Quality of life, pain and fatigue information will be collected before, during and after implementation of the activity program. The main objective is to demonstrate improved life satisfaction, decreased pain and decreased fatigue (with evidenced gathered at three consecutive periods and geographical locations through Quality of Life, Pain and Fatigue surveys). The intended sample size is 57 women.

Interventions

Activities will include physical, social, emotional, sensory and spiritual activities.

Sponsors

University of the Sciences in Philadelphia
CollaboratorOTHER
M.D. Anderson Cancer Center
CollaboratorOTHER
Temple University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women diagnosed with cancer * Age of 21 of older * Clearance from their MD to participate in the activity program

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Change in Canadian Occupational Performance Measure Scores at Day1, Day 5 and Week 6Day 1, Day 5 and week 6Individualized, client-centered measure designed for use by occupational therapists to detect change in a client's self-perception of occupational performance and satisfaction over time

Secondary

MeasureTime frameDescription
Change in Brief Pain InventoryDay 1, Day 5, and week 6Pain assessment that measures level of pain will be reported for Day 1, Day 5, and Week 6
Change in Brief Fatigue InventoryDay 1, Day 5, and week 6Fatigue assessment that measures level of Fatigue will be reported for Day 1, Day 5, and Week 6

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026