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

Not Applicable
Completed
Conditions
Cancer
Interventions
Other: Camp Discovery
Registration Number
NCT02802787
Lead Sponsor
Temple University
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
92
Inclusion Criteria
  • Women diagnosed with cancer
  • Age of 21 of older
  • Clearance from their MD to participate in the activity program
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Camp DiscoveryCamp DiscoveryOne week activity based camp
Primary Outcome Measures
NameTimeMethod
Change in Canadian Occupational Performance Measure Scores at Day1, Day 5 and Week 6Day 1, Day 5 and week 6

Individualized, 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 Outcome Measures
NameTimeMethod
Change in Brief Pain InventoryDay 1, Day 5, and week 6

Pain 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 6

Fatigue assessment that measures level of Fatigue will be reported for Day 1, Day 5, and Week 6

Trial Locations

Locations (1)

Community in Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

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