Terminé

Effectiveness of an Integrated Adventure-Based Training and Health Education Programme in Promoting the Adoption and Maintenance of Regular Physical Activity Among Childhood Cancer Survivors

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Ce qui est testé

health talk and adventure-based training

+ Placebo control

Comportemental
Qui peut participer

Néoplasmes

De 7 à 18 ans
+6 critères d'éligibilité
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Soins de support

Groupe Placebo
Interventionnel
Date de début : janvier 2012
Voir le détail du protocole

Résumé

Sponsor principalThe University of Hong Kong
Dernière mise à jour : 26 avril 2016
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 1 janvier 2012

Date à laquelle le premier participant a commencé l'étude.

The aim of this study was to examine the effectiveness of an integrated adventure-based training and health education programme in promoting the exercise behavior changes, enhancing the physical activity levels, self-efficacy, reducing fatigue and improving the quality of life of Hong Kong Chinese childhood cancer survivors. Intervention Placebo control group Participants received medical follow-up according to the schedule of the oncology units. Besides, participants received an amount of time and attention that mimicked that received by the experimental group, but which is thought not to have any specific effect on the outcome measures. They were invited to attend leisure activities organized by a community centre in four different days during the study period. Activities included cartoon film shows, handicraft workshops, chess games, health talks on the prevention of influenza and healthy diet, day visit to museum and theme park. Experimental group Besides receiving medical follow-up, participants joined a four-day integrated adventure-based training and health education programme, which contains education talks, a workshop to work out a feasible individual action plan for regular physical activity and adventure-based training activities. Previous research showed that working out individual action plan is important, which can increase the possibility for people to turn their intentions into health promotion action. The content of the education talks were tailor-made for participants in which they did not engage in regular physical activity. To ensure the dosage of intervention delivered in terms of the amount, frequency, duration, and breadth would be adequate to assess the quality and to manage outcomes, such as physical activity levels, self-efficacy, stages of change and quality of life, the following measures were taken. An advisory committee was set up with the purpose to develop an appropriate integrated programme for Hong Kong Chinese childhood cancer survivors. The committee included the researcher, an assistant professor at a local university with considerable experience of conducting psychological interventions among children, a paediatric oncologist and a oncology nurse specialist with rich experience in taking care of children with cancer, two professional adventure-based trainers and one assistant professor of Sports and Recreation Management with extensive experience and professional knowledge in conducting adventure-based training for children. In addition, the content of the programme that related to adventure-based training activities was sent to a professional adventure-based training centre for content validation. The programme was implemented on four different days within six months in a day camp training centre, such as at 2-week, 2-month, 4-month and 6-month after the day of recruitment. The programme was implemented in small group with maximum 12 participants in one group. Health education talks and workshop were implemented in between adventure-based training activities in day camp centre, which were conducted by healthcare professionals working in a local university. Adventure-based training activities were led by two qualified adventure-based training instructors with extensive experience and professional knowledge in conducting such training for children. Additionally, at least two healthcare professionals joined the adventure-based training to monitor the physical condition of the survivors and their fitness to join the adventure-based training activities. Data Collection Methods Data Collection Methods Approval for the study was obtained from the hospital ethics committees. To identify potential subjects, a leaflet containing details of the study and a demographic sheet have been mailed to all parents of childhood cancer survivors in the Sunshine Parents Club. If children and their parents are interested in the research, they can return the demographic sheet by using the enclosed return-envelop to convey their willingness to participate in the study. A briefing session will then be conducted in the out-patient clinic to those eligible children and parents. Written consent has been obtained from the parents after they were told the purposes of the study, although they were of course given the option of allowing or refusing the involvement of their child. The children has also been invited to put their names on a special children's assent form and told that their participation is voluntary. After obtaining demographic data of participants, they have been asked to respond to the Chinese version of the FS-C/FS-A, PA-SE, CUHK-PARCY, PASCQ and PedsQL. They have also been assessed for muscle strength using a hand-held dynamometer. Participants have been randomly assigned to the experimental and control groups. All participants received a telephone call inviting them to join the interventions according to their group assignment at an appointed time. Data collection has been conducted again at 3, 6, 9 and 12 months after starting the intervention. All participants has been informed that there would be home visits for data collection. Analysis The Statistical Package for Social Sciences (SPSS) software, version 19.0 for Windows will be used to analyze quantitative data. Intention-to-treat analysis will be used and missing data will be substituted by the last-observation-carried-forward procedure. The comparability of the experimental and control groups will be assessed by using inferential statistics (independent t-test and chi-squared test). Descriptive statistics will be used to calculate the mean scores and standard deviation of different scales. Mixed between-within subjects ANOVA (split-plot ANOVA) will be used to determine whether the adventure-based training programme was effective in reducing fatigue, increasing childhood cancer survivors' levels of physical activity, self-efficacy and muscle strength and enhancing their quality of life. In addition, Friedman Test will be used to determine any changes in stages of change between the experimental and control groups.

Sponsor principalThe University of Hong Kong
Dernière mise à jour : 26 avril 2016
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

71 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Soins de support

Cette étude teste des approches visant à améliorer le confort, le bien-être ou la qualité de vie des personnes atteintes d'une maladie, notamment en aidant à mieux gérer les symptômes.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

De 7 à 18 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Néoplasmes

Critères

4 critères d'inclusion nécessaires pour participer
Hong Kong Chinese childhood cancer survivors defined here as having completed treatment at least six months previously

able to speak Cantonese and read Chinese

between 7 and 18 years of age

did not engage in regular physical activity for the past 6 months

2 critères d'exclusion empêchent la participation
childhood cancer survivors with evidence of recurrence or second malignancies

those with physical impairment or cognitive and learning problems identified from their medical records

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

2 groupes d'intervention sont désignés dans cette étude

50% de chances d'être dans le groupe placebo en aveugle

Groupes de traitement

Groupe I

Expérimental
Participate will join a four-day integrated health education and adventure-based training programme, which contains education talks, workshop and adventure-based training activities. The programme will be implemented on four different days within six months in a day camp training centre. The integrated programme will be implemented in small group with maximum 15 participants in one group. Health education talks and workshop will be implemented in between adventure-based training activities in day camp centre, which will be conducted by healthcare professionals working in a local university.

Groupe II

Placebo
Participants will receive an amount of time and attention that mimicked that received by the experimental group, but which is thought not to have any specific effect on the outcome measures. They will be invited to attend leisure activities organized by a community centre in four different days during the study period. Activities will include cartoon film shows, handicraft workshops, chess games, health talks on the prevention of influenza and healthy diet, day visit to museum and theme park.

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 1 site

Queen Mary Hospital

Hong Kong, ChinaOuvrir Queen Mary Hospital dans Google Maps
Terminé1 Centres d'Étude