Nordic Pole Walking for Individuals With Cancer

Sponsor
University of Ontario Institute of Technology (Other)
Overall Status
Completed
CT.gov ID
NCT03942614
Collaborator
Lakeridge Health Corporation (Other), Southlake Regional Health Centre (Other)
8
2
24.5

Study Details

Study Description

Brief Summary

Individuals diagnosed with cancer tend to be inactive and have symptom burdens that impact quality of life. A community-based Nordic Pole Walking (NPW) program may help. The primary objective of this study was to see if it was feasible to do to a larger trial. The secondary objective was to determine the effects of NPW on physical function and health-related quality of life (HRQoL). NPW or no NPW was randomly assigned to adults with non-small cell lung, prostate, colorectal, and endometrial. Eight people were enrolled in the study with 4 in the NPW group (1 dropped out) and 4 in the no NPW group.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Nordic pole walking
N/A

Detailed Description

Individuals diagnosed with cancer tend to be inactive and have symptom burdens that impact quality of life. An individualized, community-based Nordic pole walking (NPW) program may help. The primary objective of this study was to assess feasibility using the Thabane Framework of a randomized controlled trial (RCT). The secondary objective was to determine the effects of NPW on physical function (six-minute walk test, 30-second [30-s] chair stand test, Unsupported Upper Limb Exercise Test, handgrip strength, physical activity [PA]), and health-related quality of life (HRQoL, 36-Item Short Form Health [SF-36]). The study design was an eight-week multi-centred block randomized controlled feasibility study (no blinding) comparing a NPW program (versus usual daily routine) for adults with non-small cell lung, prostate, colorectal, and endometrial cancer, from hospitals and cancer support groups.

Study Design

Study Type:
Interventional
Actual Enrollment :
8 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized Controlled TrialRandomized Controlled Trial
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Nordic Pole Walking for Individuals With Cancer: A Feasibility Study Assessing Physical Function and Health-Related Quality of Life
Actual Study Start Date :
Dec 16, 2015
Actual Primary Completion Date :
Dec 31, 2017
Actual Study Completion Date :
Dec 31, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Nordic pole walking

walking with a pair of poles customized to an individual's height and stride length

Behavioral: Nordic pole walking

No Intervention: Control

usual daily routine and activities of daily living

Outcome Measures

Primary Outcome Measures

  1. Feasibility (assessed by qualitative field notes) [8 weeks]

    Feasibility was assessed using the framework as described by: Thabane L et al (2010) A tutorial on pilot studies: the what, why and how. BMC Medical Research Methodology, vol 10. England, p 1. The Thabane Framework uses 4 criteria to measure feasibility: Process, Resources, Management and Scientific. For each criteria, detailed field notes regarding objectives and measures were maintained throughout the study. These notes on the four Thabane criteria were used to categorize the study to one of four possible outcomes: 1) stop - the study is not feasible; 2) continue, but modify the protocol - the study is feasible with modifications; 3) continue without modifications, but monitor closely - the study is feasible with close monitoring; and 4) continue without modifications - the study is feasible as is.

Secondary Outcome Measures

  1. 6-minute walk test (6MWT) [8 weeks]

    The 6MWT is a measure of submaximal functional capacity. Average healthy norms (61 to 80 years old) range from 583m (women) to 687m (men).

  2. 30-second chair stand test [8 weeks]

    The 30-s chair stand test is a measure of lower body strength. In 60 to 94 years olds, average healthy norms range from 13 (women) to 14 (men)

  3. Unsupported Upper Limb Exercise Test (UULEX) [8 weeks]

    UULEX, an incremental test that measures peak unsupported arm exercise capacity. UULEX average healthy norms (40 to 89 years old) range from 11 (women) to 12 minutes (men).

  4. Hand grip strength [8 weeks]

    average healthy norms (60 to 79 years old) ranging from 24kg (women) and 41kg

  5. Functional Assessment of Cancer Therapy-Lung (FACT-L) [8 weeks]

    The FACT-L is a measure of health-related quality of life and includes 4 general and 1 lung cancer symptom-specific domain. The general domains (27 questions) include: physical well-being (PWB), social/family well-being (SWB), emotional well-being (EWB), and functional well-being (FWB). The lung cancer symptom specific (LCS) domain (7 questions) evaluates symptoms that are commonly experienced by lung cancer patients (i.e. shortness of breath, weight loss, and chest tightness). Domain scores are then combined to calculate the Total Outcome Index (TOI) (TOI = PWB + FWB + LCS), Functional Assessment of Cancer Therapy - General (FACT-G) score (FACT G = PWB + SWB + EWB + FWB), and FACT-L score (FACT-L = FACT- G + LCS). TOI range 0 to 135 with higher score better quality of life.

  6. 36-Item Short Form Health (SF-36) Questionnaire [8 weeks]

    The SF-36 is a measure of generic health-related quality of life. It assesses 8 health concepts (scales): 1) limitations in physical activities because of health problems; 2) limitations in social activities because of physical or emotional problems; 3) limitations in usual role activities because of physical health problems; 4) bodily pain; 5) general mental health; 6) limitations in usual role activities because of emotional problems; 7) vitality; and 8) general health perceptions. Scoring is a two-step process. First, precoded numeric values are recoded per a scoring key. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores (quality of life) are 0 and 100, respectively. Scores represent the percentage of total possible score achieved. In step 2, items in the same scale are averaged together to create the 8 scale scores. More information: https://www.rand.org/health-care/surveys_tools/mos/36-item-short-form/scoring.html.

  7. International Physical Activity Questionnaire (IPAQ) [8 weeks]

    The IPAQ is a measure physical activity level. Questions ask about walking, moderate-intensity activities, vigorous-intensity activities, and sitting during the following 4 domains: a) leisure time physical activity; b) domestic and gardening activities; c) work-related physical activity; and d) transport-related physical activity. Two types of scoring were done: 1) in categories (low activity levels, moderate activity levels or high activity levels), and 2) as a continuous variable (MET minutes a week). MET minutes represent the amount of energy expended carrying out physical activity and is a multiple of a person's estimated resting energy expenditure. One MET is what is expended when at rest. To get MET minutes a week from the IPAQ walking was considered 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity 8 METS. (reference: https://ugc.futurelearn.com/uploads/files/bc/c5/bcc53b14-ec1e-4d90-88e3-1568682f32ae/IPAQ_PDF.pdf)

Other Outcome Measures

  1. Demographic information [baseline]

    A data collection form was used to collect demographic information including cancer diagnosis and treatments, side effects, general health history, and smoking status (baseline only). No formal scale was used to collect this information; only descriptive information was collected.

  2. Resting heart rate [baseline and 8 weeks]

    beats per minute

  3. Oxygen saturation [baseline and 8 weeks]

    in %

  4. Height [baseline and 8 weeks]

    meters

  5. Weight [baseline and 8 weeks]

    meters

  6. Body mass index [baseline and 8 weeks]

    calculated as height divided by weight squared

  7. Bicep circumferences [baseline and 8 weeks]

    cm

  8. Chest circumference [baseline and 8 weeks]

    cm

  9. Waist circumference [baseline and 8 weeks]

    cm

  10. Hip circumference [baseline and 8 weeks]

    cm

  11. Thigh circumferences [baseline and 8 weeks]

    cm

Eligibility Criteria

Criteria

Ages Eligible for Study:
55 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • a primary diagnosis (including reoccurrence) of histologically confirmed stage I-IV NSCLC, prostate, colorectal, or endometrial cancer (with any concurrent cancer treatment)

  • a cancer diagnosis or treatment within the last three years

  • ≥ 55 years old

  • approval by the primary treating physician

  • ability to communicate in English.

Exclusion Criteria:

• engaged in NPW within the last six-months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Ontario Institute of Technology
  • Lakeridge Health Corporation
  • Southlake Regional Health Centre

Investigators

None specified.

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Mika Nonoyama, Assistant Professor, University of Ontario Institute of Technology
ClinicalTrials.gov Identifier:
NCT03942614
Other Study ID Numbers:
  • 15-018
First Posted:
May 8, 2019
Last Update Posted:
May 8, 2019
Last Verified:
May 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mika Nonoyama, Assistant Professor, University of Ontario Institute of Technology

Study Results

No Results Posted as of May 8, 2019