Effects of a stress management program on vital exhaustion and depression in women with coronary heart disease: a randomized controlled intervention study.


Journal Article

OBJECTIVES: Psychosocial factors, including depression and vital exhaustion (VE) are associated with adverse outcome in coronary heart disease (CHD). Women with CHD are poor responders to psychosocial treatment and knowledge regarding which treatment modality works in them is limited. This randomized controlled clinical study evaluated the effect of a 1-year stress management program, aimed at reducing symptoms of depression and VE in CHD women. DESIGN: Patients were 247 women, < or =75 years, recruited consecutively after a cardiac event and randomly assigned to either stress management (20 2-h sessions) and medical care by a cardiologist, or to obtaining usual health care as controls. Measurements at; baseline (6-8 weeks after randomization), 10 weeks (after 10 intervention sessions), 1 year (end of intervention) and 1-2 years follow-up. RESULTS: For VE, intention to treat analysis showed effects for time (P < 0.001) and time x treatment interaction (P = 0.005), reflecting that both groups improved over time, and that the decrease of VE was more pronounced in the intervention group. However, the level of VE was higher in the intervention group than amongst controls at baseline, 22.7 vs. 19.4 (P = 0.036) but it did not differ later. The change in depressive symptoms did not differ between the groups. CONCLUSIONS: CHD women attending our program experienced a more pronounced decrease in VE than controls. However, as they had higher baseline levels, due to regression towards the mean we cannot attribute the decrease in VE to the intervention. Whether the program has long-term beneficial effects needs to be evaluated.

Full Text

Duke Authors

Cited Authors

  • Koertge, J; Janszky, I; Sundin, O; Blom, M; Georgiades, A; László, KD; Alinaghizadeh, H; Ahnve, S

Published Date

  • March 2008

Published In

Volume / Issue

  • 263 / 3

Start / End Page

  • 281 - 293

PubMed ID

  • 18067552

Pubmed Central ID

  • 18067552

Electronic International Standard Serial Number (EISSN)

  • 1365-2796

Digital Object Identifier (DOI)

  • 10.1111/j.1365-2796.2007.01887.x


  • eng

Conference Location

  • England